Cancer patients frequently develop cachexia, a debilitating condition reflected by weight loss and skeletal muscle wasting. The negative effects that tumors exert on bone health represents a growing interest amongst cachexia researchers. Recent clinical and pre-clinical evidence demonstrates cancer-induced bone loss, even in the absence of skeletal metastases. Together with muscle wasting, losses in bone demonstrates the impact of cancer on the musculoskeletal system. Identifying therapeutic targets that comprehensively protect musculoskeletal health is essential to improve the quality of life in cancer patients and survivors. IL-6, RANKL, PTHrP, sclerostin, and TGF-β superfamily members represent potential targets to counteract cachexia. However, more research is needed to determine the efficacy of these targets in protecting both skeletal muscle and bone.
Keyphrases
- bone loss
- skeletal muscle
- papillary thyroid
- healthcare
- bone mineral density
- public health
- mental health
- weight loss
- squamous cell
- insulin resistance
- soft tissue
- squamous cell carcinoma
- bone regeneration
- human health
- bariatric surgery
- young adults
- health promotion
- immune response
- lymph node metastasis
- body composition
- risk assessment
- oxidative stress
- postmenopausal women
- transcription factor
- body mass index
- transforming growth factor
- endothelial cells
- signaling pathway
- diabetic rats
- toll like receptor
- weight gain
- obese patients
- high glucose
- genome wide identification