Evidence map›Paper›PMID 22237119›Full record

ArticleZhongguo fei ai za zhi = Chinese journal of lung cancer2012

[Expression and its clinical significance of SLC22A18 in non-small cell lung cancer].

Ming Lei, Qingshu Cheng, Yachao Zhao, Tao Liu, Xuejiao Wang, Yingchun Deng, Jing Yang, Zhipei Zhang

Open access · greenAbstract readEnglish Abstract
In one paragraph

Article in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
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  4. The Roles of ImprintedCancers · 2020
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4 · The record

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5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Ming LeiDepartment of Thoracic Surgery, Tangdu Hospital, the Fourth Military Medical University, Xi'an 710038, China.
Qingshu Cheng
Yachao Zhao
Tao Liu
Xuejiao Wang
Yingchun Deng
Jing Yang
Zhipei Zhang
Air Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveIt has been proven that multidrug resistance (MDR) is the main cause of chemotherapy failure in lung cancer. Research on emergence mechanisms of MDR has great clinical significance in improving the curative efficiency of lung cancer chemotherapy. Proteins encoded by the SLC22A18 gene, which is similar to the transmembrane transporter, may influence the sensitivity of chemotherapeutics as well as the metabolism and growth of cells. In addition, these proteins probably have some effect on the development of lung cancer MDR. The aim of the present study is to investigate the expression of SLC22A18 protein in non-small cell lung cancer (NSCLC) as well as in corresponding normal lung tissue. Furthermore, the relationship between SLC22A18 expression and pathological grade and TNM stage is analyzed.

methodsThe expression of SLC22A18 was detected by EnVinsion in 96 cases with NSCLC and in corresponding normal lung tissue. Statistical analysis was performed using SPSS 17.0 statistical software.

resultsSLC22A18 was mainly located in cell membrane and cytoplasm. The expression level of SLC22A18 in NSCLC was significantly higher than that in normal tissue (P<0.01). The positive rates in squamous cell lung cancer and lung adenocarcinoma were 68% and 78.2%, respectively (P<0.05). Moreover, the higher expression of SLC22A18 was associated with lower histological grade and later TNM stage (P<0.05).

conclusionSLC22A18 protein is overexpressed in NSCLC, and its expression is correlated with pathological grade and TNM stage. These findings provide the experimental basis for investigating the role of tumor and chemoresistance.

Indexed as

AdultAgedCarcinoma, Non-Small-Cell LungFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMiddle AgedNeoplasm StagingOrganic Cation Transport ProteinsOrganic Cation Transport ProteinsSLC22A18 protein, human

Identifiers

PMID22237119
PMCPMC5999959
OpenAlexW1488891060

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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.