Research output: Contribution to journal › Article › peer-review
Anthony Cheung, Heather J Bax, Debra H Josephs, Kristina M Ilieva, Giulia Pellizzari, Matthew Fittall, Anita Grigoriadis, Mariangela Figini, Silvana Canevari, James F Spicer, Andrew N Tutt, Sophia N Karagiannis
Original language | English |
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Journal | Oncotarget |
DOIs | |
Accepted/In press | 19 May 2016 |
Published | 27 May 2016 |
Targeting folate receptor alpha_CHEUNG_Accepted19May2016_GOLD VoR
9651_147008_2_PB.pdf, 2.46 MB, application/pdf
Uploaded date:09 Jun 2016
Version:Final published version
Licence:CC BY
Promising targeted treatments and immunotherapy strategies in oncology and advancements in our understanding of molecular pathways that underpin cancer development have reignited interest in the tumor-associated antigen Folate Receptor alpha (FRα). FRα is a glycosylphosphatidylinositol (GPI)-anchored membrane protein. Its overexpression in tumors such as ovarian, breast and lung cancers, low and restricted distribution in normal tissues, alongside emerging insights into tumor-promoting functions and association of expression with patient prognosis, together render FRα an attractive therapeutic target. In this review, we summarize the role of FRα in cancer development, we consider FRα as a potential diagnostic and prognostic tool, and we discuss different targeted treatment approaches with a specific focus on monoclonal antibodies. Renewed attention to FRα may point to novel individualized treatment approaches to improve the clinical management of patient groups that do not adequately benefit from current conventional therapies.
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