Metabolic reprogramming in cancer: Mechanisms and therapeutics
S Nong, X Han, Y Xiang, Y Qian, Y Wei, T Zhang… - MedComm, 2023 - Wiley Online Library
Cancer cells characterized by uncontrolled growth and proliferation require altered
metabolic processes to maintain this characteristic. Metabolic reprogramming is a process …
metabolic processes to maintain this characteristic. Metabolic reprogramming is a process …
Factors mediating spaceflight-induced skeletal muscle atrophy
Skeletal muscle atrophy is a well-known consequence of spaceflight. Because of the
potential significant impact of muscle atrophy and muscle dysfunction on astronauts and …
potential significant impact of muscle atrophy and muscle dysfunction on astronauts and …
Mitochondrial dysfunction and skeletal muscle atrophy: Causes, mechanisms, and treatment strategies
Skeletal muscle, which accounts for approximately 40% of total body weight, is one of the
most dynamic and plastic tissues in the human body and plays a vital role in movement …
most dynamic and plastic tissues in the human body and plays a vital role in movement …
[HTML][HTML] Regulation of myogenic gene expression
C Vicente-García, JD Hernández-Camacho… - Experimental Cell …, 2022 - Elsevier
Skeletal muscle development and regeneration is governed by the combined action of Myf5,
MyoD, Mrf4 and MyoG, also known as the myogenic regulatory factors (MRFs). These …
MyoD, Mrf4 and MyoG, also known as the myogenic regulatory factors (MRFs). These …
Functions and regulatory mechanisms of lncRNAs in skeletal myogenesis, muscle disease and meat production
S Wang, J Jin, Z Xu, B Zuo - Cells, 2019 - mdpi.com
Myogenesis is a complex biological process, and understanding the regulatory network of
skeletal myogenesis will contribute to the treatment of human muscle related diseases and …
skeletal myogenesis will contribute to the treatment of human muscle related diseases and …
Non-coding RNA regulates the myogenesis of skeletal muscle satellite cells, injury repair and diseases
Y Zhao, M Chen, D Lian, Y Li, Y Li, J Wang, S Deng… - Cells, 2019 - mdpi.com
Skeletal muscle myogenesis and injury-induced muscle regeneration contribute to muscle
formation and maintenance. As myogenic stem cells, skeletal muscle satellite cells have the …
formation and maintenance. As myogenic stem cells, skeletal muscle satellite cells have the …
[HTML][HTML] lncRNA DLEU2 acts as a miR-181a sponge to regulate SEPP1 and inhibit skeletal muscle differentiation and regeneration
Y Wang, ZJ Zhao, XR Kang, T Bian, ZM Shen… - Aging (Albany …, 2020 - ncbi.nlm.nih.gov
Sarcopenia is a serious public health problem associated with the loss of muscle mass and
function. The purpose of this study was to identify molecular markers and construct a ceRNA …
function. The purpose of this study was to identify molecular markers and construct a ceRNA …
The functional role of long non-coding RNA in myogenesis and skeletal muscle atrophy
K Hitachi, M Honda, K Tsuchida - Cells, 2022 - mdpi.com
Skeletal muscle is a pivotal organ in humans that maintains locomotion and homeostasis.
Muscle atrophy caused by sarcopenia and cachexia, which results in reduced muscle mass …
Muscle atrophy caused by sarcopenia and cachexia, which results in reduced muscle mass …
Muscle unloading: A comparison between spaceflight and ground‐based models
Prolonged unloading of skeletal muscle, a common outcome of events such as spaceflight,
bed rest and hindlimb unloading, can result in extensive metabolic, structural and functional …
bed rest and hindlimb unloading, can result in extensive metabolic, structural and functional …
Inhibition of lncRNA MAAT controls multiple types of muscle atrophy by cis-and trans-regulatory actions
J Li, T Yang, H Tang, Z Sha, R Chen, L Chen, Y Yu… - Molecular Therapy, 2021 - cell.com
Muscle atrophy is associated with negative outcomes in a variety of diseases. Identification
of a common therapeutic target would address a significant unmet clinical need. Here, we …
of a common therapeutic target would address a significant unmet clinical need. Here, we …