Literature DB >> 19216843

Jak2 inhibitors: rationale and role as therapeutic agents in hematologic malignancies.

Jacqueline Sayyah1, Peter P Sayeski.   

Abstract

Although the Jak2-V617F mutation has generated strong awareness because of its causative role in myeloproliferative disorders, reports of Jak2 gene aberrations linked to hematologic malignancies have preceded those of V617F by nearly a decade. These malignant mutations include Jak2 amino acid substitutions, deletions, insertions, and chromosomal translocations. As a consequence, researchers are increasingly focused on identifying Jak2 inhibitors that suppress aberrant Jak2 kinase activity. Some of these inhibitors may one day become therapeutically beneficial for individuals with Jak2-related hematologic malignancies. This review summarizes various Jak2 mutations associated with hematologic malignancies and assesses some of the Jak2 inhibitors in the preclinical phase or in clinical trials. By reviewing these specific areas, we hope to have a better understanding of Jak2's role in hematologic malignancies and to shed light on the utility of Jak2 inhibitors.

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Year:  2009        PMID: 19216843      PMCID: PMC2805456          DOI: 10.1007/s11912-009-0018-2

Source DB:  PubMed          Journal:  Curr Oncol Rep        ISSN: 1523-3790            Impact factor:   5.075


  47 in total

1.  Autoinhibition of Jak2 tyrosine kinase is dependent on specific regions in its pseudokinase domain.

Authors:  Pipsa Saharinen; Mauno Vihinen; Olli Silvennoinen
Journal:  Mol Biol Cell       Date:  2003-04       Impact factor: 4.138

2.  Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2.

Authors:  Stefan Joos; Martin Granzow; Heidi Holtgreve-Grez; Reiner Siebert; Lana Harder; José I Martín-Subero; Jürgen Wolf; Martyna Adamowicz; Thomas F E Barth; Peter Lichter; Anna Jauch
Journal:  Int J Cancer       Date:  2003-02-10       Impact factor: 7.396

3.  Transforming properties of chimeric TEL-JAK proteins in Ba/F3 cells.

Authors:  V Lacronique; A Boureux; R Monni; S Dumon; M Mauchauffé; P Mayeux; F Gouilleux; R Berger; S Gisselbrecht; J Ghysdael; O A Bernard
Journal:  Blood       Date:  2000-03-15       Impact factor: 22.113

4.  Growth hormone signalling and apoptosis in neonatal rat cardiomyocytes.

Authors:  Y Gu; Y Zou; R Aikawa; D Hayashi; S Kudoh; T Yamauchi; H Uozumi; W Zhu; T Kadowaki; Y Yazaki; I Komuro
Journal:  Mol Cell Biochem       Date:  2001-07       Impact factor: 3.396

5.  The JAK2 inhibitor AG490 predominantly abrogates the growth of human B-precursor leukemic cells with 11q23 translocation or Philadelphia chromosome.

Authors:  N Miyamoto; K Sugita; K Goi; T Inukai; K Lijima; T Tezuka; S Kojika; M Nakamura; K Kagami; S Nakazawa
Journal:  Leukemia       Date:  2001-11       Impact factor: 11.528

6.  TEL-JAK2 transgenic mice develop T-cell leukemia.

Authors:  C Carron; F Cormier; A Janin; V Lacronique; M Giovannini; M T Daniel; O Bernard; J Ghysdael
Journal:  Blood       Date:  2000-06-15       Impact factor: 22.113

7.  Prediction of the structure of human Janus kinase 2 (JAK2) comprising JAK homology domains 1 through 7.

Authors:  Fabrizio Giordanetto; Romano T Kroemer
Journal:  Protein Eng       Date:  2002-09

8.  Lestaurtinib (CEP701) is a JAK2 inhibitor that suppresses JAK2/STAT5 signaling and the proliferation of primary erythroid cells from patients with myeloproliferative disorders.

Authors:  Elizabeth O Hexner; Cynthia Serdikoff; Mahfuza Jan; Cezary R Swider; Candy Robinson; Shi Yang; Thelma Angeles; Stephen G Emerson; Martin Carroll; Bruce Ruggeri; Pawel Dobrzanski
Journal:  Blood       Date:  2007-11-05       Impact factor: 22.113

9.  Rapid identification of JAK2 exon 12 mutations using high resolution melting analysis.

Authors:  Amy V Jones; Nicholas C P Cross; Helen E White; Anthony R Green; Linda M Scott
Journal:  Haematologica       Date:  2008-08-12       Impact factor: 9.941

10.  The JAK kinase inhibitor CP-690,550 suppresses the growth of human polycythemia vera cells carrying the JAK2V617F mutation.

Authors:  Taghi Manshouri; Alfonso Quintás-Cardama; Roberto H Nussenzveig; Amos Gaikwad; Zeev Estrov; Josef Prchal; Jorge E Cortes; Hagop M Kantarjian; Srdan Verstovsek
Journal:  Cancer Sci       Date:  2008-06       Impact factor: 6.716

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  12 in total

1.  6-Bromoindirubin-3'-oxime inhibits JAK/STAT3 signaling and induces apoptosis of human melanoma cells.

Authors:  Lucy Liu; Sangkil Nam; Yan Tian; Fan Yang; Jun Wu; Yan Wang; Anna Scuto; Panos Polychronopoulos; Prokopios Magiatis; Leandros Skaltsounis; Richard Jove
Journal:  Cancer Res       Date:  2011-05-24       Impact factor: 12.701

Review 2.  The promise of Janus kinase inhibitors in the treatment of hematological malignancies.

Authors:  Emilee Senkevitch; Scott Durum
Journal:  Cytokine       Date:  2016-10-27       Impact factor: 3.861

Review 3.  Cancer pharmacogenomics.

Authors:  S W Paugh; G Stocco; J R McCorkle; B Diouf; K R Crews; W E Evans
Journal:  Clin Pharmacol Ther       Date:  2011-07-27       Impact factor: 6.875

4.  Understanding the structural features of JAK2 inhibitors: a combined 3D-QSAR, DFT and molecular dynamics study.

Authors:  Sathya Babu; Santhosh Kumar Nagarajan; Thirumurthy Madhavan
Journal:  Mol Divers       Date:  2019-01-07       Impact factor: 2.943

5.  Zelnorm, an agonist of 5-Hydroxytryptamine 4-receptor, acts as a potential antitumor drug by targeting JAK/STAT3 signaling.

Authors:  Lei Zhang; Qiaoling Song; Xinxin Zhang; Li Li; Ximing Xu; Xiaohan Xu; Xiaoyu Li; Zhuoya Wang; Yuxi Lin; Xin Li; Mengyuan Li; Fan Su; Xin Wang; Peiju Qiu; Huashi Guan; Yu Tang; Wenfang Xu; Jinbo Yang; Chenyang Zhao
Journal:  Invest New Drugs       Date:  2019-05-14       Impact factor: 3.850

6.  Loss of Jak2 selectively suppresses DC-mediated innate immune response and protects mice from lethal dose of LPS-induced septic shock.

Authors:  Jixin Zhong; Ping Yang; Kenjiro Muta; Robert Dong; Mario Marrero; Feili Gong; Cong-Yi Wang
Journal:  PLoS One       Date:  2010-03-09       Impact factor: 3.240

7.  MLS-2384, a new 6-bromoindirubin derivative with dual JAK/Src kinase inhibitory activity, suppresses growth of diverse cancer cells.

Authors:  Lucy Liu; Nicolas Gaboriaud; Konstantina Vougogianopoulou; Yan Tian; Jun Wu; Wei Wen; Leandros Skaltsounis; Richard Jove
Journal:  Cancer Biol Ther       Date:  2013-11-01       Impact factor: 4.742

8.  Multifaceted intervention by the Hsp90 inhibitor ganetespib (STA-9090) in cancer cells with activated JAK/STAT signaling.

Authors:  David A Proia; Kevin P Foley; Tim Korbut; Jim Sang; Don Smith; Richard C Bates; Yuan Liu; Alex F Rosenberg; Dan Zhou; Keizo Koya; James Barsoum; Ronald K Blackman
Journal:  PLoS One       Date:  2011-04-14       Impact factor: 3.240

Review 9.  Redox regulation of Janus kinase: The elephant in the room.

Authors:  Roy J Duhé
Journal:  JAKSTAT       Date:  2013-08-19

10.  Combined targeting of JAK2 and Bcl-2/Bcl-xL to cure mutant JAK2-driven malignancies and overcome acquired resistance to JAK2 inhibitors.

Authors:  Michaela Waibel; Vanessa S Solomon; Deborah A Knight; Rachael A Ralli; Sang-Kyu Kim; Kellie-Marie Banks; Eva Vidacs; Clemence Virely; Keith C S Sia; Lauryn S Bracken; Racquel Collins-Underwood; Christina Drenberg; Laura B Ramsey; Sara C Meyer; Megumi Takiguchi; Ross A Dickins; Ross Levine; Jacques Ghysdael; Mark A Dawson; Richard B Lock; Charles G Mullighan; Ricky W Johnstone
Journal:  Cell Rep       Date:  2013-11-21       Impact factor: 9.423

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