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Cisplatin-induced ecDNA enhances tumor malignancy and accelerates chemoresistance acquire in gastric cancer

delete2026-07-30
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OA
AI
H
Huanbo Zhu
L
Lian Chen
L
Longtao Huangfu *
G
Gangjian Wang
H
Huixin Cai
J
Junbing Chen
X
Xiaomei Li
M
Min Liang
W
Wenmei Li
Y
Yongqi Wang
舒绍坤 cover
舒绍坤 (Shaokun Shu) *
S
Shuqin Jia *
J
Jiafu Ji *
X
Xiaofang Xing *
DOI:10.1016/j.jare.2026.07.056delete
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Abstract

Abstract

En 中文
• Chemotherapy promoted ecDNA induction in GC, a potential mechanism that may impede therapeutic efficacy, especially in non-responding patients. • Compared to primary tumor, the proportion of ecDNA was significantly higher in metastatic tumors. • Cisplatin induced the circularization of linear DNA into ecDNA by activating the DNA damage repair pathway. • EcDNA was responsible for various promoted malignant phenotypes, which can be reversed via ecDNA inhibition. • Although ecDNA inhibitors failed to reverse pre-existing chemoresistance, they were effective in slowing the adaptation to chemotherapeutic agents.
Keywords:
Gastric cancer
Extrachromosomal DNA (ecDNA)
Chemotherapy resistance
Malignancy
Drug combination
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Journal of Advanced Research cover
Journal of Advanced Research
IF:
13
Papers:
2.8K
Citations:
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P
Peking University Cancer Hospital & Institute
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116
Papers: 26
Citations: 0
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