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ZFP161 promotes colorectal cancer progression by transcriptionally activating c-MYC.

1/5 보강
Frontiers in oncology 📖 저널 OA 100% 2021: 15/15 OA 2022: 98/98 OA 2023: 60/60 OA 2024: 189/189 OA 2025: 1004/1004 OA 2026: 620/620 OA 2021~2026 2025 Vol.15() p. 1680561
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: mixed colon adenocarcinoma
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Furthermore, high expression is associated with poor survival in patients with mixed colon adenocarcinoma. These findings suggest that the regulation of by ZFP161 may represent a potential therapeutic target in -driven cancers.

Christyani G, Cai C, Feng Y, Lee H, Tu X, Zhang C, Lou Z, Kim W

📝 환자 설명용 한 줄

Zinc Finger Protein 161 (ZFP161) is a key regulator of Ataxia Telangiectasia and Rad3-related (ATR) signaling, playing a crucial role in maintaining genomic stability.

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↓ .bib ↓ .ris
APA Christyani G, Cai C, et al. (2025). ZFP161 promotes colorectal cancer progression by transcriptionally activating c-MYC.. Frontiers in oncology, 15, 1680561. https://doi.org/10.3389/fonc.2025.1680561
MLA Christyani G, et al.. "ZFP161 promotes colorectal cancer progression by transcriptionally activating c-MYC.." Frontiers in oncology, vol. 15, 2025, pp. 1680561.
PMID 41789397 ↗

Abstract

Zinc Finger Protein 161 (ZFP161) is a key regulator of Ataxia Telangiectasia and Rad3-related (ATR) signaling, playing a crucial role in maintaining genomic stability. Human ZFP161 activates , whereas its murine ortholog, ZF5, serves as a putative transcriptional repressor of . In this study, we identified ZFP161 as a direct regulator of c-MYC. We show that ZFP161 binds to the promoter region of , modulating its expression and downstream signaling pathways. Additionally, ZFP161 promotes cell proliferation and tumorigenesis through c-MYC regulation and contributes to the malignant transformation of non-cancerous retinal pigment epithelial (RPE-1) cells. Furthermore, high expression is associated with poor survival in patients with mixed colon adenocarcinoma. These findings suggest that the regulation of by ZFP161 may represent a potential therapeutic target in -driven cancers.

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