Evidence map›Paper›PMID 35682967›Full record

ArticleInternational journal of molecular sciences2022

Carboplatin-Induced Thrombocytopenia through JAK2 Downregulation, S-Phase Cell Cycle Arrest and Apoptosis in Megakaryocytes.

Yi-Hong Wu, Hsing-Yu Chen, Wei-Chin Hong, Chen-Ying Wei, Jong-Hwei Su Pang

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07586826 (A Prospective, Randomized, Open-Label, Controlled Study of Romiplostim N01 Combined With All-Trans Retinoic Acid Versus Romiplostim N01 Alone for Persistent Isolated Chemotherapy-Induced Thrombocytopenia in Patients With Complete Remission of Gynecologic, Breast, or Lung Solid Tumors), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 21% 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.

NCT07586826 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

A Prospective, Randomized, Open-Label, Controlled Study of Romiplostim N01 Combined With All-Trans Retinoic Acid Versus Romiplostim N01 Alone for Persistent Isolated Chemotherapy-Induced Thrombocytopenia in Patients With Complete Remission of Gynecologic, Breast, or Lung Solid Tumors

TypeinterventionalSponsorPeking University People's HospitalRan2025 to 2027Enrolled220ConditionsPersistent Isolated Chemotherapy-Induced Thrombocytopenia, Chemotherapy-Induced Thrombocytopenia, Gynecologic Cancers, Ovarian CancerArmsRomiplostim N01, All-trans retinoic acid
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  3. Review
  4. 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

5 authors at 2 institutions in 1 country.

Yi-Hong WuDepartment of Chinese Medicine, Chang Gung Memorial Hospital, Guishan, Taoyuan 333, Taiwan.
Hsing-Yu ChenDepartment of Chinese Medicine, Chang Gung Memorial Hospital, Guishan, Taoyuan 333, Taiwan.ORCID 0000-0001-7897-9851
Wei-Chin HongDepartment of Chinese Medicine, Chang Gung Memorial Hospital, Guishan, Taoyuan 333, Taiwan.
Chen-Ying WeiDepartment of Chinese Medicine, Chang Gung Memorial Hospital, Guishan, Taoyuan 333, Taiwan.ORCID 0000-0002-2273-6217
Jong-Hwei Su PangGraduate Institute of Clinical Medical Sciences, Chang Gung University, Guishan, Taoyuan 333, Taiwan.
Chang Gung University · TWChang Gung Memorial Hospital · TW

Funding

NTP INFORMATION SYSTEMS SUPPORT27305C0011 · NIEHS · Z-TECH CORPORATION · 2007 to 2009
$4.3M
PROVIDE RABBITS, RATS, MICE, HAMSTERS, GERBILS, GUINEA PIGS27307C0011 · NIEHS · PI BOLEN, WAYNE · 2007 to 2007
$500k
Linkou Chang Gung Memorial Hospital CMRPG5C0011NIEHS NIH HHS 27305C0011NIEHS NIH HHS 27307C0011NIEHS NIH HHS 27398C0011Standard Food Corporation SCRPD1G0171 and SCRPD1K0391
6 · The paper itself

Abstract

Chemotherapy-induced thrombocytopenia (CIT) is a common complication when treating malignancies with cytotoxic agents wherein carboplatin is one of the most typical agents causing CIT. Janus kinase 2 (JAK2) is one of the critical enzymes to megakaryocyte proliferation and differentiation. However, the role of the JAK2 in CIT remains unclear. In this study, we used both carboplatin-induced CIT mice and MEG-01 cell line to examine the expression of JAK2 and signal transducer and activator of transcription 3 (STAT3) pathway. Under CIT, the expression of JAK2 was significantly reduced in vivo and in vitro. More surprisingly, the JAK2/STAT3 pathway remained inactivated even when thrombopoietin (TPO) was administered. On the other hand, carboplatin could cause prominent S phase cell cycle arrest and markedly increased apoptosis in MEG-01 cells. These results showed that the thrombopoiesis might be interfered through the downregulation of JAK2/STAT3 pathway by carboplatin in CIT, and the fact that exogenous TPO supplement cannot reactivate this pathway.

Indexed as

MegakaryocytesThrombocytopeniaAnimalsApoptosisCarboplatinCell Cycle CheckpointsDown-RegulationJanus Kinase 2MiceSignal TransductionS PhaseSTAT3 Transcription FactorThrombopoietinCarboplatinJanus Kinase 2STAT3 Transcription FactorThrombopoietinapoptosiscarboplatincell cycleJAK2megakaryocytethrombocytopenia

Identifiers

PMID35682967
PMCPMC9181531
OpenAlexW4281783631

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.