Targeting colorectal cancer liver metastasis through repurposing metabolic and immune inhibitors: A theoretical study.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: advanced colorectal cancer (CRC) and remains a difficult challenge in oncology
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Additionally, we predict possible improvements for CRLM treatment using an immunotherapy drug like Pembrolizumab. Overall, this paper suggests potential combinations requiring experimental validation for drug repurposing to improve CRLM treatment outcomes.
Liver metastasis from colorectal cancer is a major cause of death in patients with advanced colorectal cancer (CRC) and remains a difficult challenge in oncology.
APA
Mondal M, Lahiri A, Datta A (2026). Targeting colorectal cancer liver metastasis through repurposing metabolic and immune inhibitors: A theoretical study.. Computational biology and chemistry, 120(Pt 2), 108689. https://doi.org/10.1016/j.compbiolchem.2025.108689
MLA
Mondal M, et al.. "Targeting colorectal cancer liver metastasis through repurposing metabolic and immune inhibitors: A theoretical study.." Computational biology and chemistry, vol. 120, no. Pt 2, 2026, pp. 108689.
PMID
41086644 ↗
Abstract 한글 요약
Liver metastasis from colorectal cancer is a major cause of death in patients with advanced colorectal cancer (CRC) and remains a difficult challenge in oncology. In spite of commendable developments in medical inventions, the complexity and poor prognosis of metastatic stage, alliterative strategies are required to address Colorectal cancer liver metastasis (CRLM). This paper presents a computational study on drug repurposing for CRLM using a Boolean Network model. We comprehensively analyze CRLM signaling pathways such as WNT, PI3K/AKT/mTOR, MAPK, Hedgehog, TGF-β, NF-kB, NOTCH and HGF and target them with metabolic and immune inhibitors. This study utilizes a computational analysis to evaluate single and multi-agent treatments across scenarios involving single and multiple genetic mutations. Our findings highlights the efficacy of metabolic inhibitors such as Simvastatin, Metformin, and predict compatible partner drugs to enhance their efficacy. Additionally, we predict possible improvements for CRLM treatment using an immunotherapy drug like Pembrolizumab. Overall, this paper suggests potential combinations requiring experimental validation for drug repurposing to improve CRLM treatment outcomes.
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🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
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