Evidence map›Paper›PMID 26101711›Full record

ArticleAmerican journal of cancer research2015

Aldehyde dehydrogenase 1A1 circumscribes high invasive glioma cells and predicts poor prognosis.

Sen-Lin Xu, Sha Liu, Wei Cui, Yu Shi, Qin Liu, Jiang-Jie Duan, Shi-Cang Yu, Xia Zhang, You-Hong Cui, Hsiang-Fu Kung and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. ALDEFLUOR activity, ALDH isoforms, and their clinical significance in cancers.Journal of enzyme inhibition and medicinal chemistry · 2023
    Article
  10. Article
  11. Review
  12. Article
  13. Glioma Cells Expressing High Levels of ALDH5A1 Exhibit Enhanced Migration Transcriptional Signature in Patient Tumors.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Tumour-associated CD204Neuropathology and applied neurobiology · 2022
    Article
  18. Review
  19. Article
  20. 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

11 authors at 1 institution in 1 country.

Sen-Lin XuInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Sha LiuInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Wei CuiInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Yu ShiInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Qin LiuInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Jiang-Jie DuanInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Shi-Cang YuInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Xia ZhangInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
You-Hong CuiInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Hsiang-Fu KungInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Xiu-Wu BianInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University Chongqing, 400038, China ; Key Laboratory of Tumor Immunology and Pathology of Ministry of Education China.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma is the most aggressive brain tumor with high invasiveness and poor prognosis. More reliable, sensitive and practical biomarkers to reveal glioma high invasiveness remain to be explored for the guidance of therapy. We herein evaluated the diagnostic and prognostic value of aldehyde dehydrogenase 1A1 (ALDH1A1) in the glioma specimens from 237 patients, and found that ADLH1A1 was frequently overexpressed in the high-grade glioma (WHO grade III-IV) as compared to the low-grade glioma (WHO grade I-II) patients. The tumor cells with ALDH1A1 expression were more abundant in the region between tumor and the borderline of adjacent tissue as compared to the central part of the tumor. ALDH1A1 overexpression was associated with poor differentiation and dismal prognosis. Notably, the overall and disease-free survivals of the patients who had ALDH1A1(+) tumor cells sparsely located in the adjacent tissue were much worse. Furthermore, ALDH1A1 expression was correlated with the "classical-like" (CL) subtype as we examined GBM specimens from 72 patients. Multivariate Cox regression analysis revealed that ALDH1A1 was an independent marker for glioma patients' outcome. Mechanistically, both in vitro and in vivo studies revealed that ALDH1A1(+) cells isolated from either a glioblastoma cell line U251 or primary glioblastoma cells displayed significant invasiveness, clonogenicity, and proliferation as compared to ALDH1A1(-) cells, due to increased levels of mRNA and protein for matrix metalloproteinase 2, 7 and 9 (MMP2, MMP7 and MMP9). These results indicate that ALDH1A1(+) cells contribute to the progression of glioma including invasion, proliferation and poor prognosis, and suggest that targeting ALDH1A1 may have important implications for the treatment of highly invasive glioma.

Indexed as

ALDH1A1gliomainvasionmatrix metalloproteinaseprognosis

Identifiers

PMID26101711
PMCPMC4473324
OpenAlexW2413243403

What OpenQuestion holds

Textmetadata
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.