Evidence map›Paper›PMID 41006756›Full record

ArticleBritish journal of cancer2025

An ABCC1-based risk model is effective in the diagnosis of synchronous peritoneal metastasis in advanced colorectal cancer.

Wenqing Xie, Qianxin Luo, Zhimei Ou, Wanjun Liu, Minghan Huang, Qian Wang, Ping Lan, Daici Chen

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Article in British journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Wenqing Xie *Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.ORCID http://orcid.org/0000-0002-9623-8659
Qianxin Luo *Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Zhimei Ou *Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Wanjun LiuGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Minghan HuangGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Qian WangGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Ping LanGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. lanping@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-8901-8498
Daici ChenGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. chendc3@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-8872-0592

Funding

National Natural Science Foundation of China (National Science Foundation of China) 31970703Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2022A1515012472Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2025A1515010593
6 · The paper itself

Abstract

backgroundThe presence of peritoneal metastasis (PM) in colorectal cancer (CRC) patients indicates an advanced CRC stage. Prompt diagnosis and early PM detection are difficult, and the underlying mechanisms are unclear, resulting in limited treatment options and unsatisfactory therapeutic effects. We aimed to identify applicable biomarkers for accurately diagnosing synchronous PM in CRC patients.

methodsDifferentially expressed genes between synchronous and non-synchronous PM groups were identified via label-free proteomic analysis of primary tumors from 31 CRC patients. Quantitative real-time PCR, multiplex and conventional immunohistochemistry were used to validate gene expression. We attempted to construct a logistic regression risk model for the diagnosis of PM, which was tested in a training cohort and validated in an independent cohort.

resultsUtilizing the results from multi-omics, we established an ABCC1-based risk model. In CRC patients with imaging-negative diagnoses, the model identified patients with metastases including PM (AUC = 0.892, 95% CI: 0.840-0.944) or those with PM only (AUC = 0.859, 95% CI: 0.794-0.924); these results were validated in an independent cohort of patients with metastases including PM (AUC = 0.831, 95% CI: 0.729-0.933) or PM only (AUC = 0.819, 95% CI: 0.702-0.936). In CRC patients with CEA-negative, this model more effectively distinguishes those with exclusive peritoneal involvement, with consistent results across both training (AUC = 0.913, 95% CI: 0.854-0.972) and validation (AUC = 0.869, 95% CI: 0.795-0.943) cohorts. Additionally, in CRC patients with PM, low ABCC1 may serve as a predictive marker for chemotherapy efficacy.

conclusionsThe ABCC1-based risk model effectively predicts PM in CRC, complementing traditional diagnostics. ABCC1 may serve as a predictive marker for chemotherapy efficacy in PM.

Indexed as

ATP-Binding Cassette, Sub-Family C ProteinsBiomarkers, TumorColorectal NeoplasmsPeritoneal NeoplasmsAgedFemaleHumansMaleMiddle AgedATP-Binding Cassette, Sub-Family C ProteinsBiomarkers, Tumormultidrug resistance-associated protein 1

Identifiers

PMID41006756
PMCPMC12644583

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.