Evidence map›Paper›PMID 31253168›Full record

ArticleDiagnostic pathology2019

BCL2 overexpression: clinical implication and biological insights in acute myeloid leukemia.

Jing-Dong Zhou, Ting-Juan Zhang, Zi-Jun Xu, Yu Gu, Ji-Chun Ma, Xi-Xi Li, Hong Guo, Xiang-Mei Wen, Wei Zhang, Lei Yang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
8.2field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

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  5. Frontiers in oncology · 2026
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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 5 institutions in 1 country.

Jing-Dong ZhouDepartment of Hematology, Affiliated People's Hospital of Jiangsu University, 8 Dianli Rd, 212002, Zhenjiang, Jiangsu, People's Republic of China.
Ting-Juan ZhangDepartment of Hematology, Affiliated People's Hospital of Jiangsu University, 8 Dianli Rd, 212002, Zhenjiang, Jiangsu, People's Republic of China.
Zi-Jun XuZhenjiang Clinical Research Center of Hematology, Zhenjiang, 212002, Jiangsu, People's Republic of China.
Yu GuDepartment of Hematology, Affiliated People's Hospital of Jiangsu University, 8 Dianli Rd, 212002, Zhenjiang, Jiangsu, People's Republic of China.
Ji-Chun MaZhenjiang Clinical Research Center of Hematology, Zhenjiang, 212002, Jiangsu, People's Republic of China.
Xi-Xi LiDepartment of Hematology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, People's Republic of China.
Hong GuoZhenjiang Clinical Research Center of Hematology, Zhenjiang, 212002, Jiangsu, People's Republic of China.
Xiang-Mei WenZhenjiang Clinical Research Center of Hematology, Zhenjiang, 212002, Jiangsu, People's Republic of China.
Wei ZhangDepartment of Hematology, Affiliated People's Hospital of Jiangsu University, 8 Dianli Rd, 212002, Zhenjiang, Jiangsu, People's Republic of China.
Lei YangDepartment of Hematology, Affiliated People's Hospital of Jiangsu University, 8 Dianli Rd, 212002, Zhenjiang, Jiangsu, People's Republic of China.
Xing-Hui LiuDepartment of Clinical Laboratory, Shanghai Gongli Hospital, The Second Military Medical University, Pudong New Area, Shanghai, People's Republic of China.
Jiang LinZhenjiang Clinical Research Center of Hematology, Zhenjiang, 212002, Jiangsu, People's Republic of China. 2651329493@qq.com.
Jun QianDepartment of Hematology, Affiliated People's Hospital of Jiangsu University, 8 Dianli Rd, 212002, Zhenjiang, Jiangsu, People's Republic of China. qianjun0007@hotmail.com.
Shanghai Clinical Research Center · CNJiangsu University · CNAffiliated Hospital of Jiangsu University · CNSecond Military Medical University · CNSoochow University · CN

Funding

Clinical Medical Science Development Foundation of Jiangsu University JLY20160011Medical Innovation Team of Jiangsu Province CXTDB2017002National Natural Science Foundation of China 81270630Natural Science Foundation of Jiangsu Province for Youths BK20180280Postgraduate Research & Practice Innovation Program of Jiangsu Province KYCX17_1821Postgraduate Research & Practice Innovation Program of Jiangsu Province KYCX18_2281Scientific Research Foundation of Affiliated People's Hospital of Jiangsu University for Ph.D. KFB201603Six Talent Peaks Project in Jiangsu Province 2015-WSN-115Social Development Foundation of Zhenjiang SH2016045, SH2017040, SH2018044The Key Disciplines Group Construction Project of Pudong Health Bureau of Shanghai PWZxq2017-15Zhenjiang Clinical Research Center of Hematology SS2018009
6 · The paper itself

Abstract

backgroundBCL2 protein inhibitor venetoclax (ABT-199) has been authorized by Food and Drug Administration for relapsed/refractory chronic lymphoid leukemia with 17p deletion. Although venetoclax/ABT-199 also caused cell death in acute myeloid leukemia (AML), whether it could be applied to clinical treatment needs further studies. Here, we revealed clinical implication of BCL2 overexpression in de novo adult AML, and may provide theoretical basis for targeted therapy using venetoclax.

methodsBCL2 expression was analyzed in adult AML patients from public datasets The Cancer Genome Atlas (TCGA) and confirmed by another independent cohort from our own data.

resultsBCL2 expression showed up-regulated in AML patients among TCGA data and confirmed by our own data. BCL2 overexpression was correlated with FAB-M0/M1, whereas BCL2 under-expression was related to FAB-M5. However, BCL2 expression has no effect on overall survival (OS) and leukemia-free survival (LFS) of AML patients (determined in BCL2

conclusionsBCL2 overexpression identified specific FAB subtypes of AML, but it did not affect prognosis. Patients with BCL2 overexpression did not benefit from auto/allo-HSCT among whole-cohort-AML and cytogenetically normal AML.

Indexed as

AdultAgedAged, 80 and overCohort StudiesDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMutationPrognosisProto-Oncogene Proteins c-bcl-2Up-RegulationBCL2 protein, humanProto-Oncogene Proteins c-bcl-2ABT-199/venetoclaxAMLBCL2ExpressionHSCT

Identifiers

PMID31253168
PMCPMC6599255
OpenAlexW2955294350

What OpenQuestion holds

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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.