Evidence map›Paper›PMID 36639771›Full record

ArticleCell communication and signaling : CCS2023

Lower SLC7A2 expression is associated with enhanced multidrug resistance, less immune infiltrates and worse prognosis of NSCLC.

Shanshan Jiang, Junrong Zou, Jianyu Dong, Huimian Shi, Jie Chen, Yan Li, Xianglong Duan, Wensheng Li

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Cell communication and signaling : CCS, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  5. Article
  6. Role of solute carrier transporters in ovarian cancer (Review).International journal of molecular medicine · 2025
    Review
  7. Article
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  11. Review
  12. Article
  13. Aging · 2024
    Article
  14. Review
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 7 institutions in 1 country.

Shanshan Jiang *Institute of Hematological Research, Shaanxi Provincial People's Hospital, 256 West Youyi Road, Xi'an, 71000, Shaanxi, China. ji.ang.shan.shan@163.com.
Junrong Zou *The First Affiliated Hospital of Gan'nan Medical University, Ganzhou, China.
Jianyu Dong *Breast Center, Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Huimian ShiYiling Pharmaceutical Co., Ltd, Shijiazhuang, China.
Jie ChenDepartment of Pathology, Shaanxi Provincial People's Hospital, 256 West Youyi Road, Xi'an, 71000, Shaanxi, China.
Yan LiShaanxi Provincial Key Laboratory of Infection and Immune Diseases, Shaanxi Provincial People's Hospital, Xi'an, China.
Xianglong DuanSecond Department of General Surgery, Shaanxi Provincial People's Hospital, 256 West Youyi Road, Xi'an, 71000, Shaanxi, China. duanxianglong@nwpu.edu.cn.
Wensheng LiInstitute of Medical Research, Northwestern Polytechnical University, Xi'an, China. liwensheng263@sohu.com.
Shanxi Medical University · CNFirst Affiliated Hospital of Gannan Medical University · CNNanfang Hospital · CNNorthwestern Polytechnical University · CNShaanxi Provincial People's Hospital · CNShaanxi Provincial People's Hospital · CNShijiazhuang Yiling Pharmaceutical (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSolute carrier family 7 member 2 (SLC7A2), a cationic amino acid transporter, is lowly expressed in ovarian and hepatocellular cancers, which is associated with their worse prognosis. However, its roles in the prognosis, drug resistance and immune infiltration in non-small-cell lung cancer (NSCLC) are unclear.

methodsWe chose SLC7A2 from RNA-Seq of paclitaxel/cisplatin-resistant A549 cells, then bioinformatics, cell lines construction, RT-qPCR, and CCK8 were performed to investigate SLC7A2 role.

resultWe analyzed the 223 differentially expressed genes (DEGs) from RNA-Seq of paclitaxel/cisplatin-resistant A549 cells and found that SLC7A2 expression was down-regulated in NSCLC. Lower SLC7A2 expression was associated with worse recurrence-free survival (RFS) in NSCLC. SLC7A2 silencing enhanced the proliferation of NSCLC cells and their insensitivity to paclitaxel, cisplatin, and gemcitabine in vitro. Activation of AMPK has up-regulated SLC7A2 expression and enhanced the sensitivity of NSCLC cells to anti-tumor drugs, which could be attributed to E2F1's regulation. In addition, the levels of SLC7A2 expression were correlated to the numbers of infiltrated neutrophils, macrophages, dendritic cells and their marker genes, like CD86, HLA-DPA1 and ITGAM.

conclusionsSLC7A2 may act as a tumor suppressor to modulate drug sensitivity, immune infiltration and survival in NSCLC. Video abstract.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAmino Acid Transport Systems, BasicCell Line, TumorCisplatinDrug Resistance, MultipleDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansPaclitaxelAmino Acid Transport Systems, BasicCisplatinPaclitaxelSLC7A2 protein, humanAMPKImmune infiltrationMultiple drug resistanceNSCLCSLC7A2

Identifiers

PMID36639771
PMCPMC9838041
OpenAlexW4315865905

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.