Evidence map›Paper›PMID 32444962›Full record

ArticleJournal of cancer research and clinical oncology2020

Comprehensive analysis of the HOXA gene family identifies HOXA13 as a novel oncogenic gene in kidney renal clear cell carcinoma.

Yuanbo Cui, Ming Yan, Chunyan Zhang, Jinhui Xue, Quanwu Zhang, Shanshan Ma, Fangxia Guan, Wei Cao

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

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  20. Pan-cancer analysis identifies ESM1 as a novel oncogene for esophageal cancer.Esophagus : official journal of the Japan Esophageal Society · 2021
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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

8 authors at 2 institutions in 1 country.

Yuanbo Cui *Department of Translational Medicine Center, Zhengzhou Central Hospital Affiliated To Zhengzhou University, Zhengzhou, 450007, China. cuiyuanbo18@126.com.ORCID http://orcid.org/0000-0002-8201-4216
Ming Yan *Basic Medical College, Zhengzhou University, Zhengzhou, 450001, China.
Chunyan ZhangDepartment of Clinical Laboratory, Zhengzhou Central Hospital Affiliated To Zhengzhou University, Zhengzhou, 450007, China.
Jinhui XueDepartment of Pathology, Zhengzhou Central Hospital Affiliated To Zhengzhou University, Zhengzhou, 450007, China.
Quanwu ZhangDepartment of Pathology, Zhengzhou Central Hospital Affiliated To Zhengzhou University, Zhengzhou, 450007, China.
Shanshan MaSchool of Life Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Fangxia GuanSchool of Life Sciences, Zhengzhou University, Zhengzhou, 450001, China. fxguan@126.com.
Wei CaoDepartment of Translational Medicine Center, Zhengzhou Central Hospital Affiliated To Zhengzhou University, Zhengzhou, 450007, China. caoweiyu@hotmail.com.
Zhengzhou Central Hospital · CNZhengzhou University · CN

Funding

the Key Scientific and Technological Project in Henan Province 182102310328the Key Scientific Research Projects of Institutions of Higher Learning in Henan Province 20A310018the Provincial Co-construction Project of Medical Science and Technology in Henan SB201903032
6 · The paper itself

Abstract

objectivesKidney renal clear cell carcinoma (KIRC) is one of the most common lethal cancers in the human urogenital system. As members of the Homeobox (HOX) family, Homeobox-A (HOXA) cluster genes have been reported to be involved in the development of many cancer types. However, the expression and clinical significance of HOXA genes in KIRC remain largely unknown. MATERIALS AND

methodsIn this study, we comprehensively analyzed the mRNA expression and prognostic values of HOXA genes in KIRC using The Cancer Genome Atlas (TCGA) analysis databases online. Colony formation assay, flow cytometry and Western blot were used to detect cell proliferation, apoptosis, cell cycle, and protein level of the indicated gene.

resultsWe found that the HOXA genes were differentially expressed in KIRC tissues when compared with normal tissues. The expression of HOXA4 and HOXA13 were significantly up-regulated, while HOXA7 and HOXA11 were down-regulated in KIRC. High mRNA levels of HOXA2, HOXA3 and HOXA13, and low level of HOXA7 predicted poor overall survival (OS) of KIRC patients. High mRNA level of HOXA13 further indicated a poor disease-free survival (DFS) of KIRC patients. Functionally, knockdown of HOXA13 significantly suppressed cell proliferation of KIRC in vitro, increased the protein level of p53 and decreased the protein level of cyclin D1 in KIRC cells. Over-expression of HOXA13 had the opposite effects on KIRC cells.

conclusionCollectively, our findings suggest that HOXA13 functions as a novel oncogene in KIRC and may be a potential biomarker for this malignancy.

Indexed as

Biomarkers, TumorCarcinoma, Renal CellCell Line, TumorCell ProliferationCyclin D1Databases, GeneticDown-RegulationGene Knockdown TechniquesHomeodomain ProteinsHumansKidney NeoplasmsMultigene FamilyOncogenesRNA, MessengerTranscription FactorsTranscription, GeneticBiomarkers, TumorCCND1 protein, humanCyclin D1homeobox protein HOXA13Homeodomain ProteinsHOXA4 protein, humanHOXA7 protein, humanRNA, MessengerTP53 protein, humanTranscription FactorsTumor Suppressor Protein p53Homeobox-A cluster genesHOXA13Kidney renal clear cell carcinomaOncogenePrognosis

Identifiers

PMID32444962
PMCPMC11804755
OpenAlexW3028132277

What OpenQuestion holds

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Registered trials

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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.