Evidence map›Paper›PMID 37292284›Full record

ArticleHeliyon2023

TMEM2 induces epithelial-mesenchymal transition and promotes resistance to temozolomide in GBM cells.

Lun Gao, Shiao Tong, Junhui Liu, Jiayang Cai, Zhang Ye, Long Zhou, Ping Song, Zhiyang Li, Pan Lei, Hangyu Wei and 3 more

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. 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

13 authors at 2 institutions in 1 country.

Lun GaoDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Shiao TongDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Junhui LiuDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Jiayang CaiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Zhang YeDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Long ZhouDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Ping SongDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Zhiyang LiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Pan LeiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Hangyu WeiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Qiuwei HuaDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Daofeng TianDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Qiang CaiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China.
Wuhan University · CNRenmin Hospital of Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most common intracranial malignant tumor and is notorious for its poor prognosis. An important element in the short overall survival of GBM patients is the lack of understanding the pathogenesis and progression of tumor and deficiency biomarkers that can be used for early diagnosis and therapeutic sensitivity monitoring. Studies have shown that transmembrane protein 2 (TMEM2) is participated in tumorigenesis of various human tumors, including rectal and breast cancers. Although Qiuyi Jiang et al. have reported that TMEM2 combined with IDH1/2 and 1p19q can predict the survival time of glioma patients based on bioinformatics, its expression and biological role of glioma remain unclear. In our study, we investigated the effect of TMEM2 expression level on glioma malignancy in public datasets and an independent internal dataset. We revealed TEMM2 expression was higher in GBM tissues than in non-tumor brain tissues (NBT). Moreover, the increase in TMEM2 expression level was closely related to tumor malignancy. The survival analysis showed that TMEM2 high expression reduces survival time in all glioma patients, including GBM and LGG patients. Subsequent experiments demonstrated that knockdown TMEM2 inhibited proliferation of GBM cells. In addition, we analyzed TMEM2 mRNA levels in different GBM subtypes, and demonstrated that TMEM2 expression was upregulated in mesenchymal subtype. Meanwhile, bioinformatics analysis and transwell assay indicated that knockdown TMEM2 suppressed epithelial-mesenchymal transition (EMT) in GBM. Importantly, Kaplan-Meier analysis demonstrated that TMEM2 high expression reduced the treatment response to TMZ in GBM patients. Knockdown of TMEM2 alone did not reduce apoptosis GBM cells, but significant apoptotic cells were observed in the group treated with additional TMZ. These studies may contribute to improving the accuracy of early diagnosis and evaluating the effectiveness of TMZ treatment in GBM patients.

Indexed as

EMTPrognosisProliferationTMEM2TMZ

Identifiers

PMID37292284
PMCPMC10245174
OpenAlexW4378070569

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.