Evidence map›Paper›PMID 36539562›Full record

ArticleMolecular biology reports2023

Evaluation of the gene encoding carnitine transporter (OCTN2/SLC22A5) expression in human breast cancer and its association with clinicopathological characteristics.

Negar Dinarvand, Farzaneh Karimi, Reza Azizi, Sedighe Rastaghi, Abdolkarim Sheikhi, Morteza Pourfarzam

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Article in Molecular biology reports, 2023. 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
0.3field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

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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

6 authors at 5 institutions in 1 country.

Negar DinarvandHyperlipidemia Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Farzaneh KarimiDepartment of Physiology, Behbahan Faculty of Medical Sciences, Behbahan, Iran.
Reza AziziMolecular and Medicine Research Center, Khomein University of Medical Sciences, Khomein, Iran.
Sedighe RastaghiDepartment of Biostatistics, School of Public Health, Mashhad University of Medical Sciences, Mashhad, Iran.
Abdolkarim SheikhiDepartment of Immunology, School of Medicine, Dezful University of Medical Sciences, Dezful, Iran.
Morteza PourfarzamDepartment of Clinical Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran. pourfarzam@pharm.mui.ac.ir.ORCID http://orcid.org/0000-0002-9563-8044
Ahvaz Jundishapur University of Medical Sciences · IRDezful University of Medical Sciences · IRImam Khomeini Hospital · IRIsfahan University of Medical Sciences · IRMashhad University of Medical Sciences · IR

Funding

Dezful University of Medical Sciences 1396.35Isfahan University of Medical Sciences 396510
6 · The paper itself

Abstract

backgroundFatty acid oxidation (FAO) is a major energy-generating process in the mitochondria and supports proliferation, growth, and survival of cancer cells. L-Carnitine is an essential co-factor for carrying long-chain fatty acids into the mitochondria. The entry of l-carnitine across cell membrane is regulated by OCTN2 (SLC22A5). Thus, it can plays a significant role in the mitochondrial fatty acid oxidation. This study aimed to evaluate the OCTN2 expression and its association with clinicopathological characteristics in breast cancer.

methodsIn this work, OCTN2 was examined in 54 pairs of fresh samples of breast cancer (BC) and adjacent noncancerous tissue using quantitative real-time polymerase chain reaction and immunohistochemistry (IHC). The IHC approach was also used to investigate the expression of additional clinicopathological features.

resultsThe present research findings revealed that the relative expression of OCTN2 in BC tissues was substantially higher than the adjacent normal tissues. This up-regulation was correlated positively with tumor size and Ki-67 and negatively with the progesterone receptor (PR) status, providing evidence of the opposite effects of OCTN2 and PR on tumor development.

conclusionThe study shows that the OCTN2 expression in BC patients may be used as a prognostic biomarker and a tumor oncogene. As a result, it could be considered a possible therapeutic target. Nevertheless, the significance of the findings needs to be confirmed by further studies.

Indexed as

Breast NeoplasmsOrganic Cation Transport ProteinsCarnitineFatty AcidsFemaleHumansSolute Carrier Family 22 Member 5CarnitineFatty AcidsOrganic Cation Transport ProteinsSLC22A5 protein, humanSolute Carrier Family 22 Member 5Breast cancerFatty acid oxidationOCTN2

Identifiers

PMID36539562
OpenAlexW4312066313

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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.