Evidence map›Paper›PMID 38992586›Full record

ArticleBMC gastroenterology2024

The expression and clinical significance of CFAP65 in colon cancer.

Yunze Li, Dongmei Ran, Shiva Basnet, Buzhe Zhang, Hongjing Pei, Chenchen Dan, Zixuan Zhang, Liang Zhang, Tianyu Lu, Yifan Peng and 1 more

Abstract read
In one paragraph

Article in BMC gastroenterology, 2024. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Yunze Li *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Unit III & Ostomy Service, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, 52 Fucheng Road, Beijing, 100142, P.R. China.
Dongmei Ran *Department of Pathology, Southern University of Science and Technology Hospital, Shenzhen, 518055, Guangdong, China.
Shiva BasnetKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Unit III & Ostomy Service, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, 52 Fucheng Road, Beijing, 100142, P.R. China.
Buzhe ZhangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Unit III & Ostomy Service, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, 52 Fucheng Road, Beijing, 100142, P.R. China.
Hongjing PeiKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Unit III & Ostomy Service, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, 52 Fucheng Road, Beijing, 100142, P.R. China.
Chenchen DanKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Unit III & Ostomy Service, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, 52 Fucheng Road, Beijing, 100142, P.R. China.
Zixuan ZhangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Unit III & Ostomy Service, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, 52 Fucheng Road, Beijing, 100142, P.R. China.
Liang ZhangDepartment of Gastroenterology, Southern University of Science and Technology Hospital, Shenzhen, 518055, Guangdong, China.
Tianyu LuDepartment of Gastroenterology, Southern University of Science and Technology Hospital, Shenzhen, 518055, Guangdong, China.
Yifan PengDepartment of Unit III & Ostomy Service, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Beijing, 100142, P.R. China. pengyf_1972@aliyun.com.
Changzheng DuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Unit III & Ostomy Service, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, 52 Fucheng Road, Beijing, 100142, P.R. China. ducz@sustech.edu.cn.

Funding

National Natural Science Foundation of China 32170590Shenzhen Science and Technology Research and Development Fund JCYJ20220530113814033
6 · The paper itself

Abstract

backgroundCFAP65 (cilia and flagella associated protein 65) is a fundamental protein in the development and formation of ciliated flagella, but few studies have focused on its role in cancer. This study aimed to investigate the prognostic significance of CFAP65 in colon cancer.

methodsThe functionally enriched genes related to CFAP65 were analyzed through the Gene Ontology (GO) database. Subsequently, CFAP65 expression levels in colon cancer were evaluated by reverse transcription and quantitative polymerase chain reaction (RT-qPCR) and immunoblotting in 20 pairs of frozen samples, including tumors and their matched paratumor tissue. Furthermore, protein expression of CFAP65 in 189 colon cancer patients were assessed via immunohistochemical staining. The correlations between CFAP65 expression and clinical features as well as long-term survival were statistically analyzed.

resultsCFAP65-related genes are significantly enriched on cellular processes of cell motility, ion channels, and GTPase-associated signaling. The expression of CFAP65 was significantly higher in colon cancer tissue compared to paratumor tissue. The proportion of high expression and low expression of CFAP65 in the clinical samples of colon cancer were 61.9% and 38.1%, respectively, and its expression level was not associated with the clinical parameters including gender, age, tumor location, histological differentiation, tumor stage, vascular invasion and mismatch repair deficiency. The five-year disease-free survival rate of the patients with CFAP65 low expression tumors was significantly lower than that those with high expression tumors (56.9% vs. 72.6%, P = 0.03), but the overall survival rate has no significant difference (69% vs. 78.6%, P = 0.171). The cox hazard regression analysis model showed that CFAP65 expression, tumor stage and tumor location were independent prognostic factors.

conclusionsIn conclusion, we demonstrate CFAP65 is a potential predictive marker for tumor progression in colon cancer.

Indexed as

Biomarkers, TumorColonic NeoplasmsAgedClinical RelevanceFemaleHumansMaleMembrane ProteinsMicrofilament ProteinsMiddle AgedNeoplasm ProteinsPrognosisBiomarkers, TumorFXYD3 protein, humanMembrane ProteinsMicrofilament ProteinsNeoplasm ProteinsCFAP65Colon cancerPathologyPrognosisSurgery

Identifiers

PMID38992586
PMCPMC11238475

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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.