Article citationsMore>>
Misale, S., Yaeger, R., Hobor, S., Scala, E., Janakiraman, M., Liska, D., Valtorta, E., Schiavo, R., Buscarino, M., Siravegna, G., Bencardino, K., Cercek, A., Chen, C.T., Veronese, S., Zanon, C., Sartore-Bianchi, A., Gambacorta, M., Gallicchio, M., Vakiani, E., Boscaro, V., Medico, E., Weiser, M., Siena, S., Di Nicolantonio, F., Solit, D. and Bardelli, A. (2012) Emergence of KRAS Mutations and Acquired Resistance to Anti-EGFR Therapy in Colorectal Cancer. Nature, 486, 532-536.
https://doi.org/10.1038/nature11156
has been cited by the following article:
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TITLE:
Sequential and Dual Inhibition of Pleiotropic Targets in Cancer—A Novel Strategy to Sensitize Tumor Cells to Targeted Therapies and Overcome Resistance
AUTHORS:
M. Nezami
KEYWORDS:
Targeted Therapies, Multitargeted Epigenetic Therapy, Oncogenic Addiction, Tumor Resistance, Tyrosine Kinase
JOURNAL NAME:
Journal of Cancer Therapy,
Vol.10 No.2,
February
21,
2019
ABSTRACT: In this paper we discuss the rationale of applying a “sequential”
targeted therapy with a specific application in clinical practice, given our
understanding of cancer heterogenous and dynamic biology. We explore the
advantages of “single inhibition” to combinational therapies and dual
inhibition on key pathways, as well as a multi-step approach to use
“oncological addiction” and “oncogenic shock” as a suicide plan for cancer. We specifically
explain how the downstream targets can be used to “create” feedback loops in an
advantage for creating actionable targets in upstream signaling molecules. We
apply this hypothesis in the clinical setting, with superior outcomes shown in
a series of case studies. We conclude that “sequential and dual inhibition” can
be considered a meaningful approach to checkmate the tumor, with minimum chance of tumor resistance. We recommend further clinical studies to generate
further hypotheses based on each actionable target.
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