Literature DB >> 17133113

Ba/F3 cells and their use in kinase drug discovery.

Markus Warmuth1, Sungjoon Kim, Xiang-ju Gu, Gang Xia, Francisco Adrián.   

Abstract

PURPOSE OF REVIEW: Due to their ability to function as dominant oncogenes, protein kinases have become favored targets in the quest for 'molecularly-targeted' cancer chemotherapeutics. The discovery of a large number of cancer-associated mutations in the kinome, and the progress in developing specific small-molecule kinase inhibitors has increased the need for accurate, reproducible, and efficient kinase activity-dependent cellular assay systems. RECENT
FINDINGS: Ba/F3, a murine interleukin-3 dependent pro-B cell line is increasingly popular as a model system for assessing both the potency and downstream signaling of kinase oncogenes, and the ability of small-molecule kinase inhibitors to block kinase activity. Facilitated by their growth properties, Ba/F3 cells have recently been adapted to high-throughput assay formats for compound profiling. Further, several published approaches show promise in predicting resistance to small-molecule kinase inhibitors elicited by point mutations interfering with inhibitor binding.
SUMMARY: Ba/F3 cells are an increasingly popular tool in kinase drug discovery. The ability to test the transforming capacity of newly identified kinase mutations, and to profile drug candidates and compound libraries in high-throughput fashion, combined with the use of Ba/F3 cells to predict clinical resistance will greatly facilitate developments in this field.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17133113     DOI: 10.1097/CCO.0b013e328011a25f

Source DB:  PubMed          Journal:  Curr Opin Oncol        ISSN: 1040-8746            Impact factor:   3.645


  87 in total

1.  Development of a siRNA and shRNA screening system based on a kinase fusion protein.

Authors:  Sofie Pieraets; Luk Cox; Olga Gielen; Jan Cools
Journal:  RNA       Date:  2012-04-26       Impact factor: 4.942

2.  Intracellular delivery of bioactive molecules using light-addressable nanocapsules.

Authors:  Kimberly A D Gregersen; Zachary B Hill; Jennifer C Gadd; Bryant S Fujimoto; Dustin J Maly; Daniel T Chiu
Journal:  ACS Nano       Date:  2010-11-30       Impact factor: 15.881

3.  Akt shows variable sensitivity to an Hsp90 inhibitor depending on cell context.

Authors:  Maria A Theodoraki; Mary Kunjappu; David W Sternberg; Avrom J Caplan
Journal:  Exp Cell Res       Date:  2007-07-06       Impact factor: 3.905

Review 4.  Targeting cancer with small molecule kinase inhibitors.

Authors:  Jianming Zhang; Priscilla L Yang; Nathanael S Gray
Journal:  Nat Rev Cancer       Date:  2009-01       Impact factor: 60.716

5.  A non-covalent inhibitor XMU-MP-3 overrides ibrutinib-resistant BtkC481S mutation in B-cell malignancies.

Authors:  Fu Gui; Jie Jiang; Zhixiang He; Li Li; Yunzhan Li; Zhou Deng; Yue Lu; Xinrui Wu; Guyue Chen; Jingyi Su; Siyang Song; Yue-Ming Zhang; Cai-Hong Yun; Xin Huang; Ellen Weisberg; Jianming Zhang; Xianming Deng
Journal:  Br J Pharmacol       Date:  2019-12-09       Impact factor: 8.739

Review 6.  Mechanisms of drug resistance in kinases.

Authors:  Rina Barouch-Bentov; Karsten Sauer
Journal:  Expert Opin Investig Drugs       Date:  2011-02       Impact factor: 6.206

7.  Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer.

Authors:  Hengyu Lu; Nicole Villafane; Turgut Dogruluk; Caitlin L Grzeskowiak; Kathleen Kong; Yiu Huen Tsang; Oksana Zagorodna; Angeliki Pantazi; Lixing Yang; Nicholas J Neill; Young Won Kim; Chad J Creighton; Roel G Verhaak; Gordon B Mills; Peter J Park; Raju Kucherlapati; Kenneth L Scott
Journal:  Cancer Res       Date:  2017-05-16       Impact factor: 12.701

8.  Efficacy and Tolerability of Pyrazolo[1,5-a]pyrimidine RET Kinase Inhibitors for the Treatment of Lung Adenocarcinoma.

Authors:  Casey J N Mathison; Donatella Chianelli; Paul V Rucker; John Nelson; Jason Roland; Zhihong Huang; Yang Yang; Jiqing Jiang; Yun Feng Xie; Robert Epple; Badry Bursulaya; Christian Lee; Mu-Yun Gao; Jennifer Shaffer; Sergio Briones; Yelena Sarkisova; Anna Galkin; Lintong Li; Nanxin Li; Chun Li; Su Hua; Shailaja Kasibhatla; Jacqueline Kinyamu-Akunda; Rie Kikkawa; Valentina Molteni; John E Tellew
Journal:  ACS Med Chem Lett       Date:  2020-02-12       Impact factor: 4.345

9.  Paradoxical activation and RAF inhibitor resistance of BRAF protein kinase fusions characterizing pediatric astrocytomas.

Authors:  Angela J Sievert; Shih-Shan Lang; Katie L Boucher; Peter J Madsen; Erin Slaunwhite; Namrata Choudhari; Meghan Kellet; Phillip B Storm; Adam C Resnick
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-26       Impact factor: 11.205

10.  Cellular Ser/Thr-kinase assays using generic peptide substrates.

Authors:  Deanna G Adams; Yu Wang; Puiying A Mak; Jason Chyba; Orzala Shalizi; Jason Matzen; Paul Anderson; Tim R Smith; Michael Garcia; Genevieve L Welch; Emmanuel J Claret; Michel Fink; Anthony P Orth; Jeremy S Caldwell; Achim Brinker
Journal:  Curr Chem Genomics       Date:  2008-05-23
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.