Evidence map›Paper›PMID 31646201›Full record

ArticleBiochemistry and biophysics reports2019

CMTM6, the newly identified PD-L1 regulator, correlates with PD-L1 expression in lung cancers.

Feng Gao, Jing Chen, Jia Wang, Peixiang Li, Sheng Wu, Jue Wang, Yong Ji

Open access · goldAbstract read
In one paragraph

Article in Biochemistry and biophysics reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. CMTM6 as a master regulator of PD-L1.Cancer immunology, immunotherapy : CII · 2022
    Review
  7. The clinical and prognostic significance of CMTM6/PD-L1 in oncology.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  8. CMTM6, a potential immunotherapy target.Journal of cancer research and clinical oncology · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
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

7 authors at 2 institutions in 1 country.

Feng GaoDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, 214500, China.
Jing ChenDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, 214500, China.
Jia WangDepartment of Neurology, The Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, 212001, China.
Peixiang LiDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, 214500, China.
Sheng WuDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, 214500, China.
Jue WangDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, 214500, China.
Yong JiDepartment of Pathology, Jingjiang People's Hospital, Jingjiang, Jiangsu, 214500, China.
First People's Hospital of Jingzhou · CNJiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modulation of Immune check point regulators, especially the PD-1/PD-L1 axis, plays a critical role in successful management of a small proportion of lung cancer patients, but not so effective in the rest of lung cancer patients. A better understanding of immunotherapy non-responsive or resistant patients therefore warranted for future development of novel therapeutics. The newly identified regulator CMTM6 (CKLF-like MARVEL transmembrane domain containing 6) has been reported to serves as the stabilizer of PD-L1 and enhances the inhibitory effect of PD-L1 on immune system in both cell line and animal models, but its clinical relevance associated with PD-L1 is unknown and the current study is designed to address this question. The study using immunohistochemistry demonstrated that CMTM6 positivity from 15 out of 19 types of cancers with our in-house tissue microarray, and PD-L1 expression is always found only in CMTM6 positive cancers. CMTM6 and PD-L1 expression were analyzed in 81 lung cancer patient sample, and we observed that CMTM6 expression correlated with cancer histotypes and inversely correlated with cancer metastases, but not with patients' age and gender. No PD-L1 expression was observed in negative CMTM6 samples. Higher expression PD-L1 is also associated with higher CMTM6 expression. In summary, CMTM6 expression is associated with PD-L1 expression, as well as lung cancer histotypes and metastasis. The results thus for the first time confirmed earlier reports on CMTM6/PD-L1 connection, from a clinical aspect of analysis.

Indexed as

CMTM6ImmunohistochemistryLung carcinomasPD-L1Therapy

Identifiers

PMID31646201
PMCPMC6804456
OpenAlexW2979067999

What OpenQuestion holds

Textmetadata
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.