Literature DB >> 29895526

Potent effects of roniciclib alone and with sorafenib against well-differentiated thyroid cancer.

Shu-Fu Lin1,2, Jen-Der Lin3,2, Chuen Hsueh2,4, Ting-Chao Chou5, Richard J Wong6.   

Abstract

Activation of cyclin-dependent kinase activity is frequently observed in many human cancers; therefore, cyclin-dependent kinases that promote cell cycle transition and cell proliferation may be potential targets in the treatment of malignancy. The therapeutic effects of roniciclib, a cyclin-dependent kinase inhibitor for papillary and follicular thyroid cancer (designated as well-differentiated thyroid cancer), were investigated in this study. Roniciclib inhibited cell proliferation in two papillary and two follicular thyroid cancer cell lines in a dose-dependent manner. Roniciclib activated caspase-3 activity and induced apoptosis. Cell cycle progression was arrested in the G2/M phase. Roniciclib treatment in vivo retarded the growth of two well-differentiated thyroid tumors in xenograft models in a dose-dependent fashion. Furthermore, the combination of roniciclib with sorafenib was more effective than either single treatment in a follicular thyroid cancer xenograft model. Acceptable safety profiles appeared in animals treated with either roniciclib alone or roniciclib and sorafenib combination therapy. These findings support roniciclib as a potential drug for the treatment of patients with well-differentiated thyroid cancer.
© 2018 Society for Endocrinology.

Entities:  

Keywords:  cyclin-dependent kinase; roniciclib; well-differentiated thyroid cancer

Mesh:

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Year:  2018        PMID: 29895526     DOI: 10.1530/ERC-18-0150

Source DB:  PubMed          Journal:  Endocr Relat Cancer        ISSN: 1351-0088            Impact factor:   5.678


  2 in total

1.  Targeting PLKs as a therapeutic approach to well-differentiated thyroid cancer.

Authors:  Shu-Fu Lin; Jen-Der Lin; Chun-Nan Yeh; Yu-Tung Huang; Ting-Chao Chou; Richard J Wong
Journal:  Endocr Relat Cancer       Date:  2019-08       Impact factor: 5.678

2.  Development of newly synthesised quinazolinone-based CDK2 inhibitors with potent efficacy against melanoma.

Authors:  Eman R Mohammed; Ghada F Elmasry
Journal:  J Enzyme Inhib Med Chem       Date:  2022-12       Impact factor: 5.051

  2 in total

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