Evidence map›Paper›PMID 27386062›Full record

ArticleCaspian journal of internal medicine2016

The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping.

Mozhagan Moazami-Goudarzi, Majid Farshdousti-Hagh, Abbasali Hoseinpour-Feizi, Mehdi Talebi, Ali Akbar Movassaghpour-Akbari, Karim Shams-Asanjan, Jamal Eyvazi-Ziyaee, Morteza Seifi

Open access · greenAbstract read
In one paragraph

Article in Caspian journal of internal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 pooled it
1.0field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 3 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Article
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  9. [Fucoxanthin induces prostate cancer PC-3 cell apoptosis by causing mitochondria dysfunction and oxidative stress].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
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  10. Observational
  11. Role of Autophagy and Apoptosis in Acute Lymphoblastic Leukemia.Cancer control : journal of the Moffitt Cancer Center
    Review
  12. 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 1 institution in 2 countries.

Mozhagan Moazami-GoudarziStem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Majid Farshdousti-HaghStem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Abbasali Hoseinpour-FeiziStem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Mehdi TalebiStem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Ali Akbar Movassaghpour-AkbariStem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Karim Shams-AsanjanStem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Jamal Eyvazi-ZiyaeeStem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Morteza SeifiStem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran.
University of Tabriz · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBCL-2 is the most important anti-apoptotic regulator and Bax is a pro-apoptotic protein. The status of these parameters or the ration of BCL-2 to BAX is important in malignant cell fate as well as normal cells.

methodsSixty-two ALL patients and 62 healthy sex-and age-matched controls were studied. After genotyping, the promoter region of the BAX and BCL-2 genes by RFLP-PCR method the patients were classified in nine prognostic groups, after that, the overall survival ratio of each score was compared with others pair-wise or between groups.

resultsThe frequencies of the AA, AC, CC alleles of the BCL-2 C-938A polymorphism in patient group were 33 (53.23%), 18 (29.03%), 11 (17.74%), and in the control group were 13 (21.0%), 27 (43.5%), 22 (35.5%), respectively (P=0.003). Also, the frequencies of AA, AG, GG alleles of the BAX G-248A SNP were 15 (24.2%), 24 (38.7%), 23 (37.1%) in ALL group and 13 (21.0%), 25 (40.3%), 24 (38.7%) (p>0.05) in the control group. The survival time estimation and ratio were significantly different between different SNPs in BCL-2 (P=0.002).

conclusionThese findings showed that the BCL-2 promoter region polymorphism is more reliable than BAX gene promoter polymorphism in any ALL scoring system. But the establishment of complete scoring system requires further more clinical and laboratory findings along with genetic polymorphisms is necessary.

Indexed as

Acute lymphoblastic LeukemiaBAXBCL2Prognostic scoringSingle Nucleotide Polymorphism.Survival

Identifiers

PMID27386062
PMCPMC4913713
OpenAlexW2345930656

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.