Evidence map›Paper›PMID 24000012›Full record

ArticleMolecular and cellular biochemistry2013

RACK1 promotes the proliferation of THP1 acute myeloid leukemia cells.

Dalin Zhang, Qingyang Wang, Ting Zhu, Junxia Cao, Xueying Zhang, Jing Wang, Xiaoqian Wang, Yan Li, Beifen Shen, Jiyan Zhang

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In one paragraph

Article in Molecular and cellular biochemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  5. Components of the JNK-MAPK pathway play distinct roles in hepatocellular carcinoma.Journal of cancer research and clinical oncology · 2023
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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

10 authors at 2 institutions in 1 country.

Dalin ZhangDepartment of Immunology, College of Basic Medical Sciences, Central South University, Changsha, 410078, People's Republic of China.
Qingyang Wang
Ting Zhu
Junxia Cao
Xueying Zhang
Jing Wang
Xiaoqian Wang
Yan Li
Beifen Shen
Jiyan Zhang
Institute of Basic Medical Sciences of the Chinese Academy of Medical SciencesCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The receptor for activated C kinase 1 (RACK1), an adaptor protein implicated in the regulation of multiple signaling pathways, has been reported to contribute to the survival of leukemic progenitor cells by enhancing the activity of glycogen synthase kinase 3β (GSK3β). However, it remains unknown whether RACK1 also contributes to the oncogenic growth of acute myeloid leukemia (AML) cells. Here, we report that transient or stable silencing of endogenous RACK1 expression by RACK1 short hairpin RNAs (shRNAs) led to impaired proliferation of THP1 AML cells without inducing terminal differentiation. Further exploration revealed that RACK1 loss-of-function resulted in reduced GSK3β activity. GSK3β shRNA treatment showed similar effects to RACK1 loss-of-function. Our data collectively suggest that RACK1 contributes to THP1 cell proliferation through, at least partially, enhancing GSK3β activity. Thus, targeting RACK1 may have some important therapeutic implications in the treatment of AML.

Indexed as

ApoptosisCell CycleCell DifferentiationCell Line, TumorCell ProliferationCell SurvivalGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGTP-Binding ProteinsHumansLeukemia, Myeloid, AcuteLipopolysaccharide ReceptorsNeoplasm ProteinsPhagocytosisReceptors, Cell SurfaceReceptors for Activated C KinaseGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGSK3B protein, humanGTP-Binding ProteinsLipopolysaccharide ReceptorsNeoplasm ProteinsRACK1 protein, humanReceptors, Cell SurfaceReceptors for Activated C KinaseRNA, Small Interfering

Identifiers

PMID24000012
OpenAlexW2085286609

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.