Literature DB >> 26810603

A novel multi-CDK inhibitor P1446A-05 restricts melanoma growth and produces synergistic effects in combination with MAPK pathway inhibitors.

Philip Eliades1,2, David M Miller1,3, Benchun Miao1, Raj Kumar1, Michael Taylor1, Shama Buch4, Sreesha P Srinivasa4, Keith T Flaherty5, Hensin Tsao1.   

Abstract

Nearly 100% of melanomas have a defect in the p16(INK4A):cyclin D-CDK4/6:RB pathway, leading to abnormal cell cycle control and unregulated cellular proliferation. Here, we report that P1446A-05, a novel multi-CDK inhibitor has significant inhibitory activity against cutaneous and uveal melanoma. Mechanistic studies revealed that P1446A-05 inhibits phosphorylation targets of CDK members, and induces cell cycle arrest and apoptosis irrespective of melanoma genotype or phenotype. Additionally, we show preclinical evidence that P1446A-05 can synergize with other small molecule inhibitors previously studied in melanoma. Collectively, these data demonstrate that targeting cell cycle and transcriptional CDKs with a small molecule multi-CDK inhibitor is a viable approach for developing novel anti-melanoma therapeutics.

Entities:  

Keywords:  Cell cycle; MAPK pathways; melanoma, multi-CDK inhibitor; synergy

Mesh:

Substances:

Year:  2016        PMID: 26810603      PMCID: PMC4970529          DOI: 10.1080/15384047.2016.1139267

Source DB:  PubMed          Journal:  Cancer Biol Ther        ISSN: 1538-4047            Impact factor:   4.742


  23 in total

Review 1.  Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies.

Authors:  Ting-Chao Chou
Journal:  Pharmacol Rev       Date:  2006-09       Impact factor: 25.468

2.  Distinct sets of genetic alterations in melanoma.

Authors:  John A Curtin; Jane Fridlyand; Toshiro Kageshita; Hetal N Patel; Klaus J Busam; Heinz Kutzner; Kwang-Hyun Cho; Setsuya Aiba; Eva-Bettina Bröcker; Philip E LeBoit; Dan Pinkel; Boris C Bastian
Journal:  N Engl J Med       Date:  2005-11-17       Impact factor: 91.245

Review 3.  To cycle or not to cycle: a critical decision in cancer.

Authors:  M Malumbres; M Barbacid
Journal:  Nat Rev Cancer       Date:  2001-12       Impact factor: 60.716

4.  The CDK4/6 inhibitor LY2835219 overcomes vemurafenib resistance resulting from MAPK reactivation and cyclin D1 upregulation.

Authors:  Vipin Yadav; Teresa F Burke; Lysiane Huber; Robert D Van Horn; Youyan Zhang; Sean G Buchanan; Edward M Chan; James J Starling; Richard P Beckmann; Sheng-Bin Peng
Journal:  Mol Cancer Ther       Date:  2014-08-13       Impact factor: 6.261

Review 5.  Cyclin-dependent kinases as therapeutic targets in melanoma.

Authors:  David M Miller; Keith T Flaherty
Journal:  Pigment Cell Melanoma Res       Date:  2014-02-10       Impact factor: 4.693

6.  Identification of K1/K10 and K5/K14 keratin pairs in human melanoma cell lines.

Authors:  Y Katagata; T Aoki; Y Hozumi; T Yoshida; S Kondo
Journal:  J Dermatol Sci       Date:  1996-12       Impact factor: 4.563

7.  p53 rescue through HDM2 antagonism suppresses melanoma growth and potentiates MEK inhibition.

Authors:  Zhenyu Ji; Ching Ni Njauw; Michael Taylor; Victor Neel; Keith T Flaherty; Hensin Tsao
Journal:  J Invest Dermatol       Date:  2011-10-13       Impact factor: 8.551

8.  The CDK Network: Linking Cycles of Cell Division and Gene Expression.

Authors:  Robert P Fisher
Journal:  Genes Cancer       Date:  2012-11

Review 9.  The cell-cycle regulator CDK4: an emerging therapeutic target in melanoma.

Authors:  Karen E Sheppard; Grant A McArthur
Journal:  Clin Cancer Res       Date:  2013-10-01       Impact factor: 12.531

10.  The anti-melanoma activity of dinaciclib, a cyclin-dependent kinase inhibitor, is dependent on p53 signaling.

Authors:  Brijal M Desai; Jessie Villanueva; Thierry-Thien K Nguyen; Mercedes Lioni; Min Xiao; Jun Kong; Clemens Krepler; Adina Vultur; Keith T Flaherty; Katherine L Nathanson; Keiran S M Smalley; Meenhard Herlyn
Journal:  PLoS One       Date:  2013-03-18       Impact factor: 3.240

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  1 in total

1.  An increased cell cycle gene network determines MEK and Akt inhibitor double resistance in triple-negative breast cancer.

Authors:  Vera E van der Noord; Ronan P McLaughlin; Marcel Smid; John A Foekens; John W M Martens; Yinghui Zhang; Bob van de Water
Journal:  Sci Rep       Date:  2019-09-16       Impact factor: 4.379

  1 in total

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