Evidence map›Paper›PMID 39264531›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2025

Investigation of TMEM41A's function in breast cancer prognosis and its connection to immune cell infiltration.

Fan Fan, Ruiwen Feng, Yuxin Zhang, Xiabin Li, Yan Tang

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Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Fan Fan *School of Public Health, Southwest Medical University, Luzhou, 646000, Sichuan, China.
Ruiwen Feng *School of Public Health, Southwest Medical University, Luzhou, 646000, Sichuan, China.
Yuxin ZhangChongqing Key Laboratory of Biomedical Engineering, College of Biomedical Engineering, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Xiabin LiDepartment of Breast Surgery, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, China.
Yan TangSchool of Public Health, Southwest Medical University, Luzhou, 646000, Sichuan, China. tangyan200310@163.com.ORCID http://orcid.org/0000-0003-1580-0134

Funding

Natural Science Foundation of Sichuan Province 2022NSFSC0741Southwest Medical University 2021ZKZD001
6 · The paper itself

Abstract

backgroundGlobally, breast cancer is the most common type of malignant tumor. It has been demonstrated that TMEM41A is abnormally expressed in a number of cancers and is linked to a dismal prognosis. TMEM41A's involvement in breast cancer remains unknown, though.

methodsData from databases such as TCGA were used in this study. Expression differences were compared using non-parametric tests. Cox regression analysis was employed, and analyses such as Nomogram were used to assess the significance of TMEM41A in predicting the prognosis of breast cancer. Lastly, it was looked into how immune cell infiltration in breast cancer is related to TMEM41A expression levels.

resultsThe results suggest that TMEM41A is overexpressed in breast cancer and correlates with poor prognosis (P = 0.01), particularly in early-stage and ductal A breast cancer (P < 0.01). Breast cancer patients' expression of TMEM41A was found to be an independent risk factor (HR = 1.132, 95% CI 1.036-1.237) by multifactorial Cox regression analysis. The Nomogram prediction model's c-index was 0.736 (95% CI 0.684-0.787). The results of GSEA biofunctional enrichment analysis included the B cell receptor signaling pathway (P < 0.05). Ultimately, there was a significant correlation (P < 0.05) between TMEM41A expression in breast cancer and an infiltration of twenty immune cells.

conclusionsBreast cancer tissues overexpress TMEM41A, which is linked to immune cell infiltration and prognosis (particularly in early stage and luminal A breast cancer). Overexpression of TMEM41A is anticipated to serve as a novel prognostic indicator and therapeutic target for breast cancer.

Indexed as

Breast NeoplasmsLymphocytes, Tumor-InfiltratingMembrane ProteinsOncogene ProteinsAdultAgedAged, 80 and overGene Expression Regulation, NeoplasticHumansMiddle AgedPrognosisMembrane ProteinsOncogene ProteinsTMEM41A protein, humanBreast cancerImmune cell infiltrationPrognosisTransmembrane protein 41A

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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.