Understanding the Role of Exercise in Cancer Cachexia Therapy

Systemic Inflammation

Systemic inflammation is present in many wasting conditions, and the associated pro-inflammatory cytokines have been used clinically during patient assessment and widely investigated as potential drivers of cancer cachexia development.^11-14 The source of elevated circulating cytokines has been attributed to both the tumor and to tumor-host immune interactions. ¹¹ The chronic elevation of inflammatory cytokines has well described actions on cellular functions in liver, adipose, and skeletal muscle.^15,16 Pro-inflammatory cytokines such as intereleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) have been implicated in cancer cachexia development in both humans and preclinical models.^15,17-21 Elevated plasma TNF-α is present in several human cancers^20,22 and has been associated with anorexia, enhanced lipolysis, and muscle atrophy in tumor bearing rodents.^23-25 While inhibiting TNF-α has demonstrated favorable results in some preclinical cancer models,^24-26 anti-TNF-α treatments in clinical trials have not prevented weight loss in cancer patients.^27,28 IL-6 also has established roles in systemic tissue dysregulation. Systemically elevated IL-6 can induce liver growth and insulin resistance,^29,30 activate adipose tissue lipolysis, ³¹ and disrupt muscle protein turnover.^32-34 IL-6 has been associated with cachexia development across several preclinical mouse models,^14,34-36 and plasma levels are inversely related to survival in metastatic lung cancer patients. ¹⁴ Treatment with an anti-IL-6 receptor neutralizing antibody (tocilizumab) improved indices of cachexia progression in lung cancer patients.^37,38 While significant advances have been made in determining the role of specific cytokines in the regulation of muscle wasting and cachexia progression, it is likely that cachexia development and progression results in part from the release of multiple cytokines.

Liver Dysfunction

Due to critical regulatory roles in systemic metabolism and metabolic function, there is a strong rationale for examining liver dysfunction as a potential driver of cancer cachexia. Specifically, liver regulation of physiological processes related to glucose, amino acid and lipid metabolism, hormone synthesis (eg, insulin-like growth factor-1), and metabolite detoxification ³⁹ could all promote cachexia. Indeed, the liver’s high metabolic activity significantly contributes (~20%) to whole-body resting energy expenditure.^40,41 Despite reductions in physical activity, energy expenditure is increased in cachectic cancer patients.^42,43 Hepatomegaly can be observed in both cancer patients and preclinical models,^44-46 and it has been associated with increased energy expenditure in colorectal cancer patients. ⁴⁶ Interestingly, IL-6 has been implicated in this regulation, as chronically elevated IL-6 can induce liver growth independent of cancer in mice. ²⁹ Additionally, enhanced liver inflammatory signaling has been associated with an increased acute phase protein response in cancer patients and preclinical models.^43-45,47,48 It has been suggested that the breakdown of less metabolically active tissues (eg, adipose and muscle) provides a substrate source for gluconeogenesis to support tumor metabolism and liver acute phase protein synthesis,^16,49 which contributes to the hypermetabolic state. Collectively, these data suggest that liver metabolic function may be a central regulator of wasting process, and targeted treatments may prevent cachexia progression.

Adipose Tissue Dysfunction

The loss and dysfunction of adipose tissue is an established component of cancer-induced wasting.^22,50 For many years adipose tissue’s potential to regulate the progression of cachexia was not fully appreciated, and the importance deemed secondary to lean tissue regulation. However, recent advances in adipose tissue biology and physiology have provided an excellent premise to investigate a more active role of adipose tissue in the regulation of cachexia. While there is emerging evidence for examining adipose tissue’s endocrine function as the source of adipokines that regulate whole-body metabolism and appetite, ⁵¹ adipose tissue dysregulation of lipolysis and lipid storage has been actively examined with cancer cachexia. White adipose tissue depletion can occur through activated hormone-sensitive lipase, decreased lipoprotein lipase activity, and reduced de novo lipogenesis.^52,53 Thus, enhanced lipolysis coupled with impaired lipid storage can elevate circulating free fatty acids and create a systemic environment that generates metabolic stress in numerous tissues, including skeletal muscle. This condition has been termed lipotoxicity. ³¹ In cachectic cancer patients, BMI has been negatively correlated to both adipose triglyceride lipase and hormone-sensitive lipase activities. ⁵⁴ Furthermore, intramyocellular lipids have been observed in cachectic cancer patients.^55,56 Excess skeletal muscle lipid exposure and storage can also contribute to insulin resistance and mitochondrial dysfunction. ³¹ Collectively, these studies demonstrate adipose tissue wasting may be an early event that has a role in the initiation of cancer cachexia,^54,57 and the prevention of inflammation-induced white adipose tissue loss may serve as a viable therapeutic target for preventing the progression of cachexia.

Hypogonadism

Hypogonadism in both males and females is often associated with cachexia progression. ² Although a decline in sex hormones has demonstrated effects on musculoskeletal homeostasis and metabolism, ⁵⁸ there are significant gaps in our understanding of hypogonadism’s regulatory role in cancer-induced wasting. To this end, the sex-specific responses and regulation are significantly understudied in the female. Indeed, sex differences in cachexia susceptibility have been reported in both cancer patients and preclinical models.^13,59,60 While not reported with all cancer types, low total or bioavailable testosterone has been reported in male cancer patients with and without weight loss.^{12,20,47,61-63} Low testosterone has also been associated with decreased survival in hypogonadal male pancreatic cancer patients. ⁴⁷ Similarly, circulating testosterone is reduced during the progression of cachexia and is correlated with muscle mass loss in tumor bearing mice. ⁶⁴ Primary and secondary hypogonadism can occur in cancer patients, and several factors associated with the pathogenesis include systemic inflammation, hormones (eg, leptin, ghrelin), opioid use, and chemotherapy.^12,61,62 While testosterone replacement can improve muscle mass and strength in healthy adults, ⁶⁵ this effect has not been established with cancer cachexia. However, a phase I, double-blinded randomized control trial (NCT00878995) has recently been completed; the results have yet to be disseminated. While androgens have established anabolic effects in muscle, the lack of tissue specificity and associated side effects has limited their use to treat cancer cachexia. Future studies evaluating selective androgen receptor modulators, which demonstrate robust anabolic activity and high tissue specificity, ⁶⁶ may provide a safer and more efficacious treatment alternative.

Muscle hormone sensitivity can be regulated by muscle androgen and estrogen receptor expression (AR and ER, respectively). ⁶⁷ AR expression is decreased in cachectic mouse skeletal muscle, ⁶⁴ but this reduction has not been established in human cancer patients. There is evidence suggesting that estrogen and the corresponding intracellular signaling pathways can modulate wasting susceptibility in both human cancer patients and preclinical cancer models. Several studies have found that male cancer patients are more susceptible to cachexia and demonstrate increased overall mortality when compared to females.^13,68,69 Furthermore, female tumor bearing mice were protected against cancer-induced cardiac atrophy, and inhibiting estrogen signaling through the ER could recapitulate the male wasting phenotype. ⁵⁹ The cardioprotective effects of estrogen may be related to reduced oxidative stress or activation of cell survival pathways ⁷⁰ ; however, this has not been investigated during cancer cachexia. Nonetheless, cachexia severity in female tumor bearing mice has also been associated with acyclicity (eg, loss of estrous cycle). ⁷¹ The protective effects of estrogen on cardiac and skeletal muscle atrophy may be related to inflammatory signaling, as we have previously found that ovariectomy increased muscle sensitivity to IL-6. ⁶⁰ Additional investigations that serve to improve our mechanistic understanding of circulating sex hormones in the regulation of wasting susceptibility are clearly warranted in both sexes.

Anemia

Anemia, a condition of reduced red blood cell quantity (hemoglobin level <12 g/dL), is common in cancer patients and can contribute to weight loss, reduced exercise capacity, and altered energy balance. ⁷² The prevalence and severity of anemia can be influenced by tumor burden and stage, which can adversely affect quality of life and increase mortality.^73,74 Additionally, the presence of anemia may also have detrimental effects on disease and cachexia progression. Anemia can be caused by hemolysis, blood loss, or impaired red blood cell production, which can be influenced by both cancer and anticancer treatment. ⁷⁵ While the mechanisms causing anemia with cancer cachexia are not well understood, increasing erythropoietin levels pharmacologically can improve hemoglobin levels and quality of life. ⁷⁶ Given the potential impact of anemia on survival and quality of life, anemia treatment has been examined in both cancer patients and preclinical models. Treatment options for anemia include blood transfusion, iron supplementation, and erythropoiesis stimulating agents.^77,78 Erythropoiesis stimulating agents such as recombinant human erythropoietin improved hemoglobin levels, maintained exercise capacity, decreased transfusion requirements, and increased functional ability in cancer patients.^79,80 Collectively, these studies demonstrate the importance of treating and accounting for the effects of anemia in the cancer patient. Further research is necessary to determine if long-term treatments to counteract anemia are sustainable and to improve our understanding of mechanisms inducing the anemic condition.

Protein Synthesis

Skeletal muscle protein synthesis can be regulated by nutrients, physical activity level, and inflammation. Protein kinase B (PKB, also known as Akt) and the mechanistic target of rapamycin complex 1 (mTORC1) have established roles for the integration of anabolic signaling initiated by growth factors, nutrients, and mechanical loading to regulate protein synthesis.^91,92,97 Growth factors such as insulin and insulin-like growth factor-1 (IGF-1) stimulate mTORC1 signaling through the activation of Akt.^91,92 Binding of insulin/IGF-1 to its respective cell surface receptor initiates tyrosine kinase activity and phosphoinositide 3-kinase (PI3K)-dependent activation of Akt through phosphoinositide-dependent kinase 1 (PDK1). The rapamycin-insensitive mTOR complex 2 (mTORC2) has also been implicated in growth factor signaling through the Akt phosphorylation. ⁹⁸ Subsequent downstream targets of activated Akt, which can control muscle protein synthesis, include tuberous sclerosis 2 (TSC2), glycogen synthase kinase-3β (GSK-3β), and proline-rich Akt substrate 40 kDa (PRAS40).^91,92 mTORC1 activation by Akt-dependent (eg, insulin) and Akt-independent (eg, mechanical loading, nutrition) processes promotes protein synthesis by phosphorylating the eukaryotic initiation factor 4E (4E-BP1) and the p70 ribosomal S6 kinase (S6K1). The hyperphosphorylation of 4E-BP1 prevents binding to eukaryotic initiation factor 4E (eIF4E) and the formation of 4E-BP1-eIF4E complex, resulting in the assembly of the eIF4F complex and translation initiation. ⁹¹ In addition, S6K1 activation by mTORC1 has been implicated in cap-dependent translation, translation elongation, and ribosomal biogenesis.^97,99,100 Several components of Akt/mTORC1 signaling and muscle protein synthesis are disrupted during cancer cachexia.

While suppressed protein synthesis has established roles in many wasting conditions, gaps remain in our understanding of suppressed muscle protein synthesis during cancer cachexia.^23,101 Disrupted basal and postprandial protein synthesis regulation could contribute to muscle loss in cachectic cancer patients. ¹⁰² While results are equivocal, there is evidence that basal muscle protein synthesis may not be altered in cancer patients.^103,104 However, these studies have limitations related to the patient population, the type and stage of the cancer, and the degree and duration of the cachectic phenotype. Nonetheless, several studies have reported an impaired muscle protein synthesis response to feeding (eg, anabolic resistance) during cancer.^105,106 While anabolic resistance has been hypothesized to play a role in age-related sarcopenia, ¹⁰⁷ further research is required to determine if anabolic resistance contributes to muscle mass loss in cachectic cancer patients.^102,108 Basal protein synthesis is reduced in preclinical models of cachexia^34,94,95 and is associated with disrupted Akt/mTORC1 signaling during cachexia progression. Muscle protein synthesis is suppressed during the initial stages of weight loss (<5% loss) and is further reduced with cachexia progression in tumor bearing mice. ⁹⁵ The suppression of muscle protein synthesis corresponds to reduced muscle IGF-1 expression and mTORC1 signaling. ⁹⁵ Collectively, these studies highlight a role for disrupted protein synthesis regulation throughout cachexia progression, which may serve as a potential therapeutic target to treat or prevent cancer cachexia.

Protein Breakdown

Accelerated protein breakdown has established roles in skeletal muscle atrophy. The 2 main proteolytic systems regulating atrophy include the ubiquitin-proteasome system (UPS) and the autophagy-lysosomal system. The degradation of protein via the UPS is a multistep process that requires a series of ATP-dependent enzymatic steps (E1, activation; E2, conjugation; E3, ligation) that conjugate ubiquitin to intracellular proteins, which are then degraded by the proteasome.^109,110 The digested peptides can then be used for cellular processes related to gluconeogenesis, protein synthesis, or energy production dependent on organismal energy demands. ¹¹¹ In wasting conditions, 2 muscle-specific E3 ubiquitin-conjugating enzymes, Atrogin-1 (also known as MAFbx) and MuRF-1, are thought to be critical for the breakdown of muscle proteins. ¹¹² The bulk of intracellular muscle proteins, particularly myofibrillar components, are degraded by the UPS during cancer cachexia. ¹⁰⁹ In contrast, cellular organelles can also be removed through the nonselective autophagy-lysosomal system, which is an ATP-independent process. Indeed, the autophagy-lysosomal system plays a critical role in the breakdown of cellular components during normal homeostasis and in response to various stimuli such as nutrient deprivation and muscle contraction. ¹¹³ Several forms of autophagy can occur in various cell types. During macroautophagy, cytosolic components (eg, organelles, glycogen) are sequestered within double-membrane vesicles (autophagosomes), which are then fused to the lysosome and the contents are degraded by hydrolases via the autolysosome.^113,114 The selective removal of mitochondria, termed mitophagy, has also been shown to play an important role in muscle homeostasis in healthy and diseased states. Thus, disrupted protein breakdown could negatively affect muscle homeostasis.

It is well established that protein breakdown is elevated during cancer cachexia, which results from both the activation of the ubiquitin proteasome and lysosomal-autophagy systems in both human and preclinical models.^115-117 In human cancer patients, there is evidence that tumor-derived factors and cytokines can induce autophagy in systemic tissues such as skeletal muscle. ¹¹⁶ During the initiation of cachexia, ATP-dependent processes drive protein breakdown, while both ATP-dependent and ATP-independent processes are activated during late-stage cachexia in tumor bearing mice. ⁹⁵ Total muscle ubiquitination, E3 ligase expression, and proteasomal subunit expression are induced during the initiation of cachexia, and are further increased during cachexia progression. ⁹⁵ Autophagy-related protein expression is also increased during late-stage cachexia across multiple preclinical models.^95,118 These findings highlight differential expression related to the ubiquitin and lysosomal-autophagy systems during the progression of cachexia. Autophagy flux, which may more accurately reflect activity, is also increased in cancer patients and preclinical models.^95,118,119 Further research is needed to determine the precise signaling pathways regulating the autophagy response in skeletal muscle. Nonetheless, the overt activation of these 2 proteolytic pathways can negatively affect muscle size, metabolic and contractile function, and substrate utilization during cancer cachexia.

Mitochondrial Function/Oxidative Capacity Regulation

Mitochondria oxidative capacity and function are important for the maintenance of muscle mass and metabolic function. The preservation of healthy mitochondria, which can directly affect muscle oxidative capacity, involves the coordinated processes related to biogenesis, dynamics, and mitophagy. ¹²⁰ Disruptions to any of these processes can alter mitochondrial structure and function and lead to impairments in muscle metabolism and contractile function. Mitochondrial biogenesis is responsible for the generation of newly synthesized mitochondria, and this highly regulated process is influenced by the peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α), a transcriptional coactivator that regulates genes involved in mitochondrial and energy metabolism. ⁹⁶ Mitochondrial dynamics, comprising fission and fusion processes, helps maintain the mitochondrial network and overall homeostasis. Fission involves the division of mitochondria and results in fragmentation, whereas fusion combines mitochondria and leads to network elongation. ¹²¹ Mitophagy, the autophagic removal of damaged or dysfunctional mitochondria, helps maintain a healthy mitochondrial network. Disruption to any of these processes can lead to altered tissue function and systemic metabolic function.

Mitochondria oxidative capacity and function are important for the maintenance of muscle mass. ⁹⁶ While altered oxidative capacity is commonly observed in preclinical models, this has not been uniformly found in cachectic cancer patients. ¹²² Nonetheless, several aspects of mitochondrial quality and function related to biogenesis, dynamics, and mitophagy are altered during the progression of cachexia. ³² Preclinical cachexia models clearly demonstrate disrupted skeletal muscle oxidative metabolism during the progression of cachexia,^32,123 and the loss of muscle oxidative capacity parallels skeletal muscle mass atrophy and disrupted protein turnover.^32,35 The suppression of PGC-1α precedes the loss of mitochondrial content (mtDNA) and protein expression (cytochrome C and COXIV) during the progression of cachexia.^32,123 Moreover, reductions in mitochondrial fusion proteins Mfn-1 and -2 (Mfn1/2) precede mitochondria loss during the initial stages of cachexia. In contrast, the induction of Fis1 occurs during late-stage cachexia.^32,123 Therefore, treatments targeting mitochondrial quality and function may improve muscle mass and function during cancer cachexia progression.

Systemic Inflammation

The elevated pro-inflammatory cytokine environment associated with cancer cachexia is a potential target for physical activity and exercise. The anti-inflammatory effects of exercise have been documented in healthy adults and those with chronic disease. Exercise can regulate several mediators of inflammation including visceral adiposity, production and secretion of anti-inflammatory cytokines from contracting muscle (termed myokines), and altered monocyte and macrophage receptor expression. ¹³⁴ Treadmill exercise could improve survival, and it prevented muscle mass loss in a metastatic tumor model. ¹³⁵ Moreover, exercise training during systemic IL-6 overexpression can prevent body weight and muscle mass loss in tumor bearing mice. ³⁵ These data further suggest that aerobic exercise training prior to and during cachexia progression can attenuate muscle mass and strength loss despite elevated systemic inflammation. Interestingly, while cancer patients demonstrate elevated systemic inflammation, IL-6 is increased following a single bout of exercise and has been implicated in mediating the anti-inflammatory effects of exercise. IL-6 can stimulate the production of the anti-inflammatory cytokines IL-1 receptor agonist (IL-1ra) and IL-10, ¹³⁶ and inhibit the production of the pro-inflammatory cytokine TNF-α. ¹³⁷ Related to exercise, the transient induction of these 2 cytokines by exercise is preceded by IL-6. ¹³⁸ Given the role of physical activity and myokines in systemic metabolism, future research is needed to understand the differential responses to acute and chronic exposure to inflammatory cytokines.

Hypogonadism

Low testosterone is associated with reduced muscle mass and function^12,64 and significantly contributes to decreased survival during cancer cachexia. ⁴⁷ Exercise has the potential to improve circulating sex hormones or muscle receptor expression. Interestingly, while exercise can regulate the systemic environment, which could also influence circulating sex hormones, muscle loading can increase muscle AR expression independent to changes in systemic hormones in both humans and rodents.^139-141 Mechanical loading and muscle growth are accompanied by increased AR concentration in rodents.^140,141 In healthy individuals, changes in muscle AR protein content correlated with resistance training induced muscle hypertrophy. ¹³⁹ While speculative, these studies suggest that loading may increase muscle’s sensitivity to circulating androgens and/or nongenomic receptor actions may cooperate with mechano-signaling pathways to improve mass regulation. Future studies are required to determine the precise molecular and functional consequences of increased AR on protein accretion in healthy and wasting skeletal muscle. Interestingly, recent findings suggest that the systemic hormone responses to acute resistance exercise may not be the key determinant for the hypertrophic growth response following exercise training,^139,142 which could have significant clinical and functional implications in hypogonadal patients or those undergoing androgen deprivation therapy (eg, prostate cancer). In support of this, eccentric contraction-induced muscle protein synthesis is not altered in castrated mice, ¹⁴³ and castration does not attenuate long-term overload-induced muscle growth in rats. ¹⁴⁴ Related to cancer, resistance exercise training can improve muscle mass and function in prostate cancer patients receiving androgen deprivation therapy. ¹⁴⁵ Collectively, these studies suggest that muscle loading/contraction can positively regulate muscle mass and function independent to circulating androgen levels, which could have significant implications in the treatment of cancer cachexia.

Anemia

Anemia is commonly observed in cancer patients and is tightly associated with reduced exercise capacity and increased fatigue. ¹⁴⁶ In healthy individuals, exercise training increases total hemoglobin and red blood cell mass by stimulating erythropoiesis, which can enhance oxygen delivery to peripheral tissues. ¹⁴⁷ While exercise can improve functional capacity, and decrease fatigue in cancer patients, whether this is related to improved erythropoiesis and red cell mass has not been mechanistically determined. Related to cancer cachexia, whether exercise is beneficial when anemia is present has been questioned, and it has been suggested that rectifying anemia prior to exercise training may be advantageous. ¹⁴⁸ In this context, exercise training could be detrimental and potentially reduce survival in exercise intolerant patients. Nonetheless, erythropoiesis stimulating agents and exercise training have been investigated in both cancer patients and preclinical models. Interestingly, while combined treatments can improve indices of oxidative capacity, EPO and exercise can independently improve distinct processes related to improved physical function (eg, anemia and muscle strength). ¹⁴⁹ Further research is needed to determine the distinct molecular mechanisms associated with improved outcomes related to exercise and combined therapies in cancer patients. Additionally, the appropriate mode, intensity, and frequency of exercise training in different types of anemia need to be established.

Muscle Protein Turnover

In healthy adults, a single bout of exercise can stimulate protein synthesis in various cellular fractions (eg, myofibrillar vs mitochondrial) and can remain elevated for several hours following contraction.^150-153 The duration and extent of this induction can be affected by variables such as the exercise type (endurance vs resistance), intensity and workload of muscle contractions, and the nutritional status during the postexercise recovery.^151,152,154 The muscle protein synthesis induction by muscle contraction or mechanical signaling corresponds to the activation of mTORC1 signaling in both humans and rodents.^151,155-157 Given that exercise can induce protein synthesis for many hours, the potential benefits of exercise for cachectic cancer patients will likely occur in the hours post exercise and coincides with enhanced nutritional responsiveness. Preclinical studies have demonstrated that cachectic muscle retains the capacity to hypertrophy after overload.^131,132 The ability of muscle contraction to induce protein synthesis has significant ramifications for cancer cachexia in which Akt/mTORC1 signaling may be disrupted.^34,95 Treadmill training during systemic IL-6 overexpression improved mTORC1 signaling in tumor bearing mice. ³⁴ Furthermore, a single bout of resistance exercise combined with protein ingestion stimulated muscle protein synthesis in prostate cancer patients on androgen deprivation. ¹⁵⁸ Given that muscle contraction can upregulate muscle IGF-1 expression, further work is needed to determine if this induction may have critical anabolic or anti-catabolic roles that extend beyond the acute exercise response.

The breakdown of damaged or dysfunctional proteins and organelles is required to maintain normal homeostasis. The UPS and the autophagy-lysosomal system have regulatory roles in skeletal muscle wasting with cancer.^110,159,160 While the targeting of aberrant protein degradation processes has been suggested as a potential treatment for cachexia, ¹⁵⁹ it is conceivable that inhibiting protein degradation processes may be detrimental to systemic metabolism and muscle function. Additionally, damaged proteins induced by contraction or mechanical loading must be removed for the successful restoration of muscle function. Indeed, muscle protein breakdown is also stimulated by both acute endurance and resistance exercise.^161-163 While acute exercise can accelerate protein turnover and may serve to replace damaged proteins, this has yet to be examined during cancer cachexia. In contrast, exercise training can decrease indices of protein breakdown in muscle, which may be related to improved protein quality in previously cachectic muscle. Indeed, voluntary wheel running decreased muscle E3 ligase mRNA expression and autophagy protein expression in tumor bearing mice. ¹¹⁸ Additionally, treadmill exercise prior to tumor inoculation decreased muscle protein breakdown in rats. ¹²⁸ While exercise-induced improvements have not been observed in all preclinical studies, ¹⁶⁴ this could be related to variables such as tumor type or exercise intensity. Nonetheless, a primary benefit of exercise on skeletal muscle appears to be the stimulation of protein turnover, thereby improving overall muscle metabolism and function. Additional studies are required to determine if these training adaptations can occur in the cachectic cancer patient.

Muscle Oxidative Metabolism

Endurance training is associated with increased mitochondrial density, capillary supply, and key metabolic enzymes in muscle. ¹⁶⁵ Repeated exercise induces the expression of several mitochondrial proteins such as PGC-1α, mitochondrial transcription factor A (TFAM), and nuclear respiratory factor (NRF), which can lead to improved muscle oxidative capacity. ¹⁶⁶ Furthermore, a single bout of exercise rapidly induces PGC-1α expression and mitochondrial-associated gene transcription.^167,168 Endurance exercise can also positively regulate mitochondrial dynamics through Mfn1/2 and Fis1 mRNA expression. ¹⁶⁹ Emerging evidence also suggests that resistance exercise can improve mitochondrial quality and function. mTORC1 associated with Yin Yang 1 (YY1) and PGC-1α signaling can increase mitochondrial gene expression and oxidative function. ¹⁷⁰ Resistance exercise also induces muscle PGC-1α protein expression. ¹⁷¹ Furthermore, improved mitochondrial respiratory capacity and mitochondrial complex protein expression have been observed in hypertrophic muscle following 12 weeks of resistance exercise training in humans. ¹⁷² Damaged or dysfunctional mitochondria removal has also been identified as an important exercise benefit. ¹²⁰ Indeed, treadmill exercise can prevent IL-6 dysregulation of mitochondrial biogenesis and dynamics in tumor bearing mice initiating cachexia. ³² However, severe cachexia can impair the induction of mitochondrial biogenesis signaling after a single bout of concentric muscle contractions. ⁸⁴ Interestingly, repeated bouts of eccentric muscle contraction improved muscle succinate dehydrogenase enzyme activity after the initiation of cachexia, ¹³³ which highlights a potential role for resistance exercise in atrophic muscle. While endurance and resistance exercise can alter specific aspects of mitochondrial quality control, further research is needed to determine the impact of these changes for the prevention of muscle wasting, and if cachectic muscle oxidative metabolism retains the plasticity to respond to exercise and muscle contraction.

American College of Sports Medicine (ACSM) Exercise Prescription for Cancer Survivors

Physical activity is an established modifiable risk factor that is associated with disease occurrence and all-cause mortality. ¹⁷³ Given the importance of physical activity for a cancer survivor’s quantity and quality of life, ¹⁷⁴ the ACSM has developed exercise guidelines for the cancer patient.^175,176 These guidelines are an extension of the US Department of Health and Human Services (US DHHS) Physical Activity Guidelines for Americans. ¹⁷⁷ The US DHHS guidelines provided generalized recommendations (eg, avoid inactivity) for individuals with chronic conditions such as cancer, ¹⁷⁷ and therefore the current ACSM recommendations for cancer patients have considerable overlap with the guidelines for healthy individuals (Table 2), which incorporate aerobic, resistance, and flexibility activities. Individuals are encouraged to perform aerobic exercise 3 to 5 days a week at a moderate (150 minutes) to vigorous (75 minutes) intensity, muscle strengthening exercises (eg, resistance training) at least 2 days a week, and incorporate stretching of major muscle groups on days other activities are performed.^175,177 Additionally, the ACSM guidelines account for cancer-specific issues (eg, contraindications to exercise, injury risk, etc), and it is highly recommended that exercise programs are adapted based on the individual’s health status, treatment history, and anticipated disease trajectory. ¹⁷⁵ For example, lower exercise volume/intensity and slower exercise progression may be required depending on cancer type or the individual’s work capacity. Nonetheless, provided the patient has no contraindications and can properly perform exercise, cancer patients are recommended the same physical activity/exercise guidelines as healthy individuals.^175,177,178 While the field of “exercise-oncology” is fairly new, these guidelines provide a rationale goal for cancer patients to engage in a structured physical activity and exercise program. Further research is necessary to determine the effectiveness of these recommendations for the prevention of cancer cachexia or the restoration of muscle mass in the wasting patient.

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Table 2.

ACSM Exercise Guidelines for Cancer Survivors ^a .

Aerobic	Resistance	Flexibility
• 150 min/week of moderate-intensity activity, or	• Muscle strengthening activities at moderate intensity >2 days/week for each muscle group	• Stretch major muscle groups and tendons on days other activities are performed
• 75 min/week of vigorous-intensity activity, or
• Equivalent combination

Abbreviation: ACSM, American College of Sports Medicine.

a

The guidelines were adapted from the US Department of Health and Human Services (US DHHS) Physical Activity Guidelines for Americans. ¹⁷⁷ In general, cancer patients are recommended a similar exercise prescription as healthy individuals provided the individual has no contraindications to exercise or a limited work capacity. However, additional supervision may be required depending on the health status or functional impairments (eg, cachexia severity, cancer type, cancer stage, etc). Lighter intensities and slower progression to greater volume/intensities are recommended.

Current Trials and Future Recommendations

The current body of research examining cancer cachexia suggests that a multimodal intervention, which encompasses exercise, nutritional, and pharmacological strategies, will likely be required to combat the condition. ¹⁷⁹ While exercise has generally shown to be beneficial for the cancer patient, it is currently not established if similar benefits can be achieved in a wasting cancer patient with a limited work capacity. To date there has only been 2 phase II randomized control trials utilizing exercise within a multimodal treatment regimen of cachectic cancer patients.^179,180 An ongoing clinical trial (NCT02330926) and a second completed clinical trial (NCT01419145) have reported the high feasibility of exercise training in advanced-stage cancer patients. ¹⁸⁰ While the study interpretations were limited by being statistically underpowered, this multimodal trial also suggested improved body weight and arm muscle mass in the treatment group. ¹⁸⁰ Additionally, a phase III randomized control trial is currently underway to determine if exercise can prevent/attenuate cachexia in cancer patients (EudraCT 2013-002282-19). The results from these studies should significantly enhance our understanding of exercise’s effects on clinically relevant outcomes (eg, muscle mass, survival) in cachectic cancer patients. It appears that both aerobic and resistance exercise programs may be beneficial for the cachectic cancer patient. Since cancer patients will likely participate in combined exercise programs, this should be investigated in future preclinical studies. Given the heterogeneity of cancer types, treatment regimens, and physical limitations during cachexia progression, an individualized exercise prescription tailored to clinically relevant outcomes has been recommended. ¹⁸¹ While the exact exercise prescription will not be identical for all cachectic cancer patients, future training studies should emphasize both aerobic and resistance exercise components and account for the patient’s limitations. Nonetheless, a multimodal therapy (eg, exercise, nutrition, cancer treatment) will likely be needed to maximally prevent cachexia and improve a cancer patient’s quantity and quality of life.