Evidence map›Paper›PMID 33555501›Full record

ArticleGenes & genomics2021

Monocarboxylate transporter 9 (MCT9) is down-regulated in renal cell carcinoma.

Ara Yoo, Hyeonhee Lee, Jinyoung Jung, Sang Seok Koh, Soojin Lee

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Article in Genes & genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 65% of its field
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Ara Yoo *Department of Microbiology and Molecular Biology, Chungnam National University, Daejeon, 34134, Republic of Korea.
Hyeonhee Lee *Department of Microbiology and Molecular Biology, Chungnam National University, Daejeon, 34134, Republic of Korea.
Jinyoung JungDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, 34134, Republic of Korea.
Sang Seok KohDepartment of Biological Sciences, Dong-A University, Busan, 49315, Republic of Korea.
Soojin LeeDepartment of Microbiology and Molecular Biology, Chungnam National University, Daejeon, 34134, Republic of Korea. leesoojin@cnu.ac.kr.ORCID http://orcid.org/0000-0002-0383-5025
Chungnam National University · KRDong-A University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe renal cell carcinoma (RCC) incidences are continuously increasing, however, their proper characterization remains difficult. Mammalian kidneys require large amounts of energy, and monocarboxylate transporter (MCT) gene family is responsible for the transport of monocarboxylic compounds across plasma membranes.

objectiveA total of 14 MCT members have been identified in humans, which show highly distinct substrate affinities and tissue distributions. To understand the yet-uncharacterized renal cancer-specific role of MCTs, we identified MCT members that are differentially regulated during the renal tumor progression.

methodsWe examined the expression level of MCT members in renal cell tumors and their relationship with survival rate of patients using a public database. Quantitative RT-PCR and northern blotting were performed to validate the expression of MCTs. Anti-MCT9 antiserum was raised in rabbit and used to examine MCT9 expression in normal and tumor tissue arrays. Effect of MCT9 overexpression on cell proliferation was measured using renal cancer cell lines.

resultsMCT9 was found to be abundantly and exclusively expressed in human kidney cells, and was highly downregulated in renal cancers. Kaplan-Meier plotter analysis revealed an increased survival rate of MCT9 high-expressing RCC patients. MCT9 proteins were detected in normal kidney tissue sections and their overexpression clearly attenuated renal cell proliferation.

conclusionsMCT9 was identified as a novel highly downregulated gene in renal cell cancer, and its overexpression clearly attenuated RCC cell proliferation. Thus, functional analysis of MCT9 may help in deciphering a yet-undiscovered kidney-specific energy metabolism during renal tumor progression.

Indexed as

Carcinoma, Renal CellCell Line, TumorCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticHumansKidneyKidney NeoplasmsMonocarboxylic Acid TransportersMonocarboxylic Acid TransportersSLC16A9 protein, humanCell proliferationEnergy metabolismExpression profileMonocarboxylate transporter 9Renal cell carcinoma

Identifiers

PMID33555501
OpenAlexW3127374919

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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.