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Evolutionary Origins of Metabolic Reprogramming in Cancer
被引:0
|作者:
Garcia-Sancha, Natalia
[1
,2
]
Corchado-Cobos, Roberto
[1
,2
]
Gomez-Vecino, Aurora
[1
,2
]
Jimenez-Navas, Alejandro
[1
,2
]
Perez-Baena, Manuel Jesus
[1
,2
]
Blanco-Gomez, Adrian
[1
,2
]
Holgado-Madruga, Marina
[2
,3
,4
]
Mao, Jian-Hua
[5
,6
]
Canueto, Javier
[1
,2
,7
]
Castillo-Lluva, Sonia
[8
,9
]
Mendiburu-Elicabe, Marina
[1
,2
]
Perez-Losada, Jesus
[1
,2
]
机构:
[1] Univ Salamanca, Inst Biol Mol & Celular Canc IBMCC CIC, CSIC, Salamanca 37007, Spain
[2] Inst Invest Biosanitaria Salamanca IBSAL, Salamanca 37007, Spain
[3] Univ Salamanca, Dept Fisiol & Farmacol, Salamanca 37007, Spain
[4] Inst Neurociencias Castilla & Leon INCyL, Salamanca 37007, Spain
[5] Lawrence Berkeley Natl Lab, Biol Syst & Engn Div, Berkeley, CA 94720 USA
[6] Lawrence Berkeley Natl Lab, Berkeley Biomed Data Sci Ctr, Berkeley, CA 94720 USA
[7] Hosp Univ Salamanca, Dept Dermatol, Paseo San Vicente 58-182, Salamanca 37007, Spain
[8] Univ Complutense, Fac Ciencias Quim, Dept Bioquim & Biol Mol, Madrid 28040, Spain
[9] Inst Invest Sanitarias San Carlos IdISSC, Madrid 28040, Spain
关键词:
cancer;
tissue repair;
inflammation;
regenerative phase;
evolution;
heritability;
intermediate phenotypes;
GENOME-WIDE ASSOCIATION;
SMOOTH MUSCLE ACTIN;
MULTIPLE SUSCEPTIBILITY LOCI;
TUMOR-ASSOCIATED MACROPHAGES;
QUANTITATIVE TRAIT LOCI;
SQUAMOUS-CELL CARCINOMA;
REGULATORY T-CELLS;
SKELETAL-MUSCLE;
MISSING HERITABILITY;
IDENTIFIES MULTIPLE;
D O I:
10.3390/ijms232012063
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Metabolic changes that facilitate tumor growth are one of the hallmarks of cancer. These changes are not specific to tumors but also take place during the physiological growth of tissues. Indeed, the cellular and tissue mechanisms present in the tumor have their physiological counterpart in the repair of tissue lesions and wound healing. These molecular mechanisms have been acquired during metazoan evolution, first to eliminate the infection of the tissue injury, then to enter an effective regenerative phase. Cancer itself could be considered a phenomenon of antagonistic pleiotropy of the genes involved in effective tissue repair. Cancer and tissue repair are complex traits that share many intermediate phenotypes at the molecular, cellular, and tissue levels, and all of these are integrated within a Systems Biology structure. Complex traits are influenced by a multitude of common genes, each with a weak effect. This polygenic component of complex traits is mainly unknown and so makes up part of the missing heritability. Here, we try to integrate these different perspectives from the point of view of the metabolic changes observed in cancer.
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