Evidence map›Paper›PMID 35201499›Full record

ArticleDiscover oncology2021

FAM65A as a novel prognostic biomarker in human tumors reveal by a pan-cancer analysis.

Wenken Liang, Chune Mo, Jianfen Wei, Wei Chen, Weiwei Gong, Jianling Shi, Xianliang Hou, Chunhong Li, Yecheng Deng, Minglin Ou

Open access · goldAbstract read
In one paragraph

Article in Discover oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Increased expression ofTranslational cancer research · 2025
    Article
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  4. Article
  5. Review
  6. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Wenken Liang *College of Life Science, Guangxi Normal University, No. 1, Yanshan Middle Road, Guilin, 541000, China.
Chune Mo *Central Laboratory, Guangxi Health Commission Key Laboratory of Glucose and Lipid Metabolism Disorders, The Second Affiliated Hospital of Guilin Medical University, No. 212, Renmin Road, Guilin, 541000, China.
Jianfen WeiCollege of Life Science, Guangxi Normal University, No. 1, Yanshan Middle Road, Guilin, 541000, China.
Wei ChenGastrointestinal Surgery, The Second Affiliated Hospital of Guilin Medical University, Guilin, 541000, China.
Weiwei GongCentral Laboratory, Guangxi Health Commission Key Laboratory of Glucose and Lipid Metabolism Disorders, The Second Affiliated Hospital of Guilin Medical University, No. 212, Renmin Road, Guilin, 541000, China.
Jianling ShiCentral Laboratory, Guangxi Health Commission Key Laboratory of Glucose and Lipid Metabolism Disorders, The Second Affiliated Hospital of Guilin Medical University, No. 212, Renmin Road, Guilin, 541000, China.
Xianliang HouCentral Laboratory, Guangxi Health Commission Key Laboratory of Glucose and Lipid Metabolism Disorders, The Second Affiliated Hospital of Guilin Medical University, No. 212, Renmin Road, Guilin, 541000, China.
Chunhong LiCentral Laboratory, Guangxi Health Commission Key Laboratory of Glucose and Lipid Metabolism Disorders, The Second Affiliated Hospital of Guilin Medical University, No. 212, Renmin Road, Guilin, 541000, China.
Yecheng DengCollege of Life Science, Guangxi Normal University, No. 1, Yanshan Middle Road, Guilin, 541000, China. dyecheng@163.com.
Minglin OuCentral Laboratory, Guangxi Health Commission Key Laboratory of Glucose and Lipid Metabolism Disorders, The Second Affiliated Hospital of Guilin Medical University, No. 212, Renmin Road, Guilin, 541000, China. minglinou@163.com.
Guilin Medical University · CNGuangxi Normal University · CN

Funding

Foundation for Innovative Research Groups of the National Natural Science Foundation of China No. 82060393the Guangxi Natural Science Foundation No. 2020GXNSFAA159124
6 · The paper itself

Abstract

backgroundFamily with sequence similarity 65 member A (FAM65A), also known as RIPOR1, is differentially expressed between human tumor and non-tumor tissues in kinds of cancers. In addition, it was reported that the product of FAM65A may be a biomarker for cholangiocarcinoma patients. However, there is still no evidence on the relationship between the FAM65A and different types of tumors. Our study is mainly for exploring the prognostic values of FAM65A in pan-cancer and for further discovering a potential therapeutics target.

methodsWe analyzed FAM65A expression, prognostic values, genetic alteration, protein phosphorylation, immune infiltration and enrichment analysis across different types of human malignant tumors based on The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) datasets. Additionally, Real-Time PCR (RT-qPCR) was performed to further confirm the roles of FAM65A in the pathogenesis of colorectal cancer.

resultsWe found that FAM65A expression was associated with the prognosis of multiple human tumors, especially colorectal cancer. Moreover, we also observed that FAM65A was highly expressed in colorectal cancer through RT-qPCR. We observed that decreasing phosphorylation level of the S351 locus in colon adenocarcinoma, uterine corpus endometrial carcinoma and lung adenocarcinoma. And the expression of FAM65A was positively related to cancer-associated fibroblasts (CAFs) infiltration in many tumors, such as colon adenocarcinoma. Therefore, FAM65A may be a potential prognostic biomarker of human tumors.

Indexed as

FAM65AGEOPan-cancerPrognostic biomarkerRIPOR1TCGA

Identifiers

PMID35201499
PMCPMC8777545
OpenAlexW4200623371

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