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Cancer Metabolism: From Cancer Cell to Cancer Cachexia

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Endocrinology and Metabolism".

Deadline for manuscript submissions: closed (30 November 2021) | Viewed by 9827

Special Issue Editors


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Guest Editor
Molecular Biotechnology Center Torino, Department of Molecular Biotechnology and Health Sciences, Universita degli Studi di Torino, Torino, Italy
Interests: mitochondria; cancer metabolism; cancer cell biology; cachexia; muscle atrophy
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Department of Translational Medicine, University of Piemonte Orientale, Novara, Italy
Interests: muscle regeneration; satellite cells; muscle atrophy; ghrelin; nutritional support; signal transduction
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear colleagues,

Metabolic alterations in cancer have been systematically linked to tumor progression, with metabolism being acknowledged as an important regulator of several biological processes. Defining the functional role of specific metabolites as signaling molecules, biosintetic intermediates, and co-factor is a key aspect to understand the functional role of metabolism in tumor biology.

Importantly, metabolic dysregulation affects not only the cancer cell itself but inflences as well the surrounging tumor microenvironment, and, ultimately, the host.

To this aim, metabolic dysfunctions are also present on a systemic level during cancer growth, contributing to cancer cachexia and muscle and fat tissue loss.

Cachexia is a life-threatening condition occurring in the majority of cancers. It is considered a marker of unfavorable prognosis, as it interferes with radio- and chemotherapy and directly accounts for at least 20% of cancer-associated deaths.

Hence, local and systemic metabolic alterations are important therapeutic targets for the treatment of both cancer and cachexia. The objective of this Special Issue is to provide new insight into the mechanisms controlling metabolic dysfunction in cancer progression and cachexia that can allow a deeper understanding of the pathology, as well as the advance of therapeutic approaches that can be utilized to contrast it.

We invite investigators to contribute with original research articles and review articles that will stimulate the comprehension of the molecular mechanisms underlying the relevance of metabolic reprogramming in the onset and progression of cancer cachexia.

Potential topics include but are not limited to:

  • Cancer-induced metabolic reprogramming in cachexia target tissues such as muscle, heart, adipose tissue;
  • Role of metabolite as signaling molecules, controlling cancer growth and cachexia;
  • Mitochondrial alterations (e.g., in fission-fusion-mitophagy, mitochondrial dynamics, ETC) in cancer and tissues affected by cancer cachexia, such as skeletal and cardiac muscle, adipose tissue, liver;
  • Oxidative stress;
  • Chemio/radiotherapy and metabolism;
  • Effects of physical exercise on cachexia and cancer therapy;
  • Alterations of host microbiota in cachexia and its effects on target tissues;
  • Calorie restriction/dietary intervention effects on cachexia;
  • Hormonal control of tissue wasting in cancer;
  • MicroRNAs affecting metabolism in cancer cachexia.

Assist. Prof. Dr. Paolo Porporato
Assist. Prof. Dr. Nicoletta Filigheddu
Guest Editors

Manuscript Submission Information

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Keywords

  • Cancer cachexia
  • Cancer metabolism
  • Therapy-induced dysfunction
  • Oxidative stress
  • Mitochondrial alterations
  • Metabolic dysfunction
  • Diet
  • Metabolic and endocrine dysfunction

Published Papers (1 paper)

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Review

14 pages, 962 KiB  
Review
Cancer Cachexia: Its Mechanism and Clinical Significance
by Hiroki Nishikawa, Masahiro Goto, Shinya Fukunishi, Akira Asai, Shuhei Nishiguchi and Kazuhide Higuchi
Int. J. Mol. Sci. 2021, 22(16), 8491; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22168491 - 06 Aug 2021
Cited by 77 | Viewed by 9267
Abstract
The term “cachexia” is derived from the Greek words kakos (bad) and hexis (habit). Cachexia is a malnutrition associated with chronic diseases such as cancer, chronic heart failure, chronic renal failure, and autoimmune diseases, and is characterized by decreased skeletal muscle mass. Cancer [...] Read more.
The term “cachexia” is derived from the Greek words kakos (bad) and hexis (habit). Cachexia is a malnutrition associated with chronic diseases such as cancer, chronic heart failure, chronic renal failure, and autoimmune diseases, and is characterized by decreased skeletal muscle mass. Cancer cachexia is quite common in patients with advanced cancer. Weight loss is also a characteristic symptom of cancer cachexia, along with decreased skeletal muscle mass. As nutritional supplementation alone cannot improve cachexia, cytokines and tumor-derived substances have been attracting attention as its relevant factors. Cancer cachexia can be also associated with reduced chemotherapeutic effects, increased side effects and treatment interruptions, and even poorer survival. In 2011, a consensus definition of cachexia has been proposed, and the number of relevant research reports has increased significantly. However, the pathogenesis of cachexia is not fully understood, and there are currently few regulatory-approved standard treatments for cachexia. The main reason for this is that multiple etiologies are involved in the development of cachexia. In this review, we will outline the current status of cachexia, the mechanisms of which have been elucidated in recent years, especially from the perspective of advanced cancer. Full article
(This article belongs to the Special Issue Cancer Metabolism: From Cancer Cell to Cancer Cachexia)
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