Cancer cachexia often occurs in malignant tumors and is a multifactorial and complex symptom characterized by wasting of skeletal muscle and adipose tissue, resulting in weight loss, poor life quality and shorter survival. The pathogenic mechanism of cancer cachexia is complex, involving a variety of molecular substrates and signal pathways. Advancements in understanding the molecular mechanisms of cancer cachexia have provided a platform for the development of new targeted therapies. Although recent outcomes of early-phase trials have showed that several drugs presented an ideal curative effect, monotherapy cannot be entirely satisfactory in the treatment of cachexia-associated symptoms due to its complex and multifactorial pathogenesis. Therefore, the lack of definitive therapeutic strategies for cancer cachexia emphasizes the need to develop a better understanding of the underlying mechanisms. Increasing evidences show that the progression of cachexia is associated with metabolic alternations, which mainly include excessive energy expenditure, increased proteolysis and mitochondrial dysfunction. In this review, we provided an overview of the key mechanisms of cancer cachexia, with a major focus on muscle atrophy, adipose tissue wasting, anorexia and fatigue and updated the latest progress of pharmacological management of cancer cachexia, thereby further advancing the interventions that can counteract cancer cachexia.
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May 2021
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Close ModalIn this issue Samantha and colleagues (pp. 1749–1767) provide insights into the underlying mechanism that governs the recognition of myo-inositol by TNYR SaPLD. The image shows an overlay of the loop conformations of four different structures. The unliganded TNYR structure is coloured magenta, in teal is the structure of the H168A mutant bound to PA, in green is the WT unliganded structure and in grey is the TNYR structure bound to phosphate. Image courtesy of Alice Vrielink.
Review Article|
May 10 2021
Cancer cachexia: molecular mechanism and pharmacological management
Yonghua Li;
Yonghua Li
*
1MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China
2Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China
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Huan Jin;
Huan Jin
*
1MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China
2Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China
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Yibing Chen;
Yibing Chen
3Genetic and Prenatal Diagnosis Center, Department of Gynecology and Obstetrics, First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, China
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Ting Huang;
Ting Huang
1MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China
2Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China
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Yanjun Mi;
4Department of Medical Oncology, Xiamen Key Laboratory of Antitumor Drug Transformation Research and Thoracic Tumor Diagnosis and Treatment, The First Affiliated Hospital of Xiamen University, Teaching Hospital of Fujian Medical University, Xiamen, China
Correspondence: Zhengzhi Zou (zouzhengzhi@m.scnu.edu.cn; zouzhengzhi@scnu.edu.cn) or Yanjun Mi (miyj77@xmu.edu.cn)
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Zhengzhi Zou
1MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China
2Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China
5Guangzhou Key Laboratory of Spectral Analysis and Functional Probes, College of Biophotonics, South China Normal University, Guangzhou 510631, China
Correspondence: Zhengzhi Zou (zouzhengzhi@m.scnu.edu.cn; zouzhengzhi@scnu.edu.cn) or Yanjun Mi (miyj77@xmu.edu.cn)
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Biochem J (2021) 478 (9): 1663–1688.
Article history
Received:
December 26 2020
Revision Received:
April 20 2021
Accepted:
April 22 2021
Citation
Yonghua Li, Huan Jin, Yibing Chen, Ting Huang, Yanjun Mi, Zhengzhi Zou; Cancer cachexia: molecular mechanism and pharmacological management. Biochem J 14 May 2021; 478 (9): 1663–1688. doi: https://doi.org/10.1042/BCJ20201009
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