Evidence map›Paper›PMID 11781350›Full record

ArticleThe Journal of clinical investigation2002

Human HTm4 is a hematopoietic cell cycle regulator.

José L Donato, Jon Ko, Jeffery L Kutok, Tao Cheng, Taro Shirakawa, Xiao-Quan Mao, David Beach, David T Scadden, Mohamed H Sayegh, Chaker N Adra

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.2field-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

38 citing papers in PubMed, 64 citations in OpenAlex.

  1. TET2 mutations improve the new European LeukemiaNet risk classification of acute myeloid leukemia: a Cancer and Leukemia Group B study.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011
    Trial
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  15. The MS4A family: counting past 1, 2 and 3.Immunology and cell biology · 2016
    Review
  16. Article
  17. Article
  18. Changes in transcriptome of macrophages in atherosclerosis.Journal of cellular and molecular medicine · 2015
    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

10 authors at 7 institutions in 3 countries.

José L DonatoDepartment of Medicine, Division of Hematology and Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, USA.
Jon Ko
Jeffery L Kutok
Tao Cheng
Taro Shirakawa
Xiao-Quan Mao
David Beach
David T Scadden
Mohamed H Sayegh
Chaker N Adra
Harvard University · USBeth Israel Deaconess Medical Center · USBoston Children's Hospital · USKyoto University · JPMassachusetts General Hospital · USSwansea University · GBUPMC Hillman Cancer Center · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI Deborah J Goff · 1985 to 2026
$330.6M
MECHANISMS OF HEMATOPOIESIS IN AIDSR01HL044851 · NHLBI · NEW ENGLAND DEACONESS HOSPITAL · PI SCADDEN, DAVID T · 1991 to 2015
$7.7M
TARGETED MANIPULATION OF STEM CELLS FOR AIDS THERAPYR01HL065909 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SCADDEN, DAVID T · 2001 to 2010
$4.6M
INDUCTION OF TRANSPLANTATION TOLERANCE BY ORAL ROUTER01AI033100 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI CARPENTER, CHARLES B · 1992 to 2002
$1.1M
CDK INHIBITORS AND STEM CELL REGULATIONK08DK002761 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHENG, TAO · 1999 to 2003
$579k
FUNCTIONAL STUDIES OF HTM4, A CD20/FCE RIB HOMOLOGUER29AI043663 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ADRA, CHAKAR N · 1998 to 2002
$365k
NCI NIH HHS P30 CA006516NCI NIH HHS P30CA6516NHLBI NIH HHS HL-44851NHLBI NIH HHS HL-65909NHLBI NIH HHS R01 HL044851NHLBI NIH HHS R01 HL065909NIAID NIH HHS AI-33100NIAID NIH HHS AI-43663NIAID NIH HHS R29 AI043663NIDDK NIH HHS K08 DK002761NIDDK NIH HHS K08 DK 02761
6 · The paper itself

Abstract

Proper control of cell cycle progression is critical for the constant self-renewal, differentiation, and homeostasis of the hematopoietic system. Cells of all types share the common cell cycle regulators. The different expression patterns of common regulators, in a broad sense, define cell-type or lineage specificity. However, there remains the possibility of hematopoietic cell cycle regulators tailored to the demands of the hematopoietic system. Here we describe a novel protein, HTm4, which serves as a hematopoietic cell cycle regulator. Our data indicate that HTm4 is expressed in hematopoietic tissues and is tightly regulated during the differentiation of hematopoietic stem cells. It binds to cyclin-dependent kinase-associated (CDK-associated) phosphatase-CDK2 (KAP-CDK2) complexes, and the three proteins demonstrate similar patterns of cellular expression in human lymphoid tissues. HTm4 stimulates the phosphatase activity of KAP, and its C-terminal region is required for binding to KAP-CDK2 complexes and the modulation of KAP activity. Overexpression of HTm4 can cause cell cycle arrest at the G(0)/G(1) phase. Thus, HTm4 is a novel hematopoietic modulator for the G(1)-S cell cycle transition.

Indexed as

CDC2-CDC28 KinasesCell Cycle ProteinsAmino Acid SequenceCell CycleCells, CulturedCyclin-Dependent Kinase 2Cyclin-Dependent Kinase Inhibitor ProteinsCyclin-Dependent KinasesDual-Specificity PhosphatasesGene Expression RegulationHematopoiesisHematopoietic Stem CellsHumansImmunohistochemistryMembrane ProteinsProtein Serine-Threonine KinasesCDC2-CDC28 KinasesCDK2 protein, humanCDKN3 protein, humanCell Cycle ProteinsCyclin-Dependent Kinase 2Cyclin-Dependent Kinase Inhibitor ProteinsCyclin-Dependent KinasesDual-Specificity PhosphatasesMembrane ProteinsMS4A3 protein, humanProtein Serine-Threonine KinasesProtein Tyrosine Phosphatases

Identifiers

PMID11781350
PMCPMC150822
OpenAlexW1998993441

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.