Potential for α-folate receptor-targeted treatment for ovarian cancer
Emerging Therapeutic Targets in Ovarian Cancer, Page: 245-258
2011
- 2Citations
- 3Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Book Chapter Description
The majority of ovarian and a percentage of many other cancers express high levels of the folate receptor (FR). Folates and clinically approved antifolate drugs are largely transported into tumours and normal tissues via the high capacity reduced-folate carrier (RFC). A new generation of antifolates and folate-drug conjugates have been discovered that are preferentially transported via FRs and, because of highly restricted expression in normal tissues, they reach their targets selectively in tumours expressing the receptors. FRs are also being exploited by the development of therapeutic antibodies, folate-conjugated drug carriers and imaging agents. The preclinical and emerging clinical data demonstrate that the α-FR is an important therapeutic target in cancer with particular relevance in non-mucinous ovarian carcinoma. © 2011 Springer Science+Business Media, LLC.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84882262564&origin=inward; http://dx.doi.org/10.1007/978-1-4419-7216-3_12; http://link.springer.com/10.1007/978-1-4419-7216-3_12; https://dx.doi.org/10.1007/978-1-4419-7216-3_12; https://link.springer.com/chapter/10.1007/978-1-4419-7216-3_12; http://www.springerlink.com/index/10.1007/978-1-4419-7216-3_12; http://www.springerlink.com/index/pdf/10.1007/978-1-4419-7216-3_12
Springer Science and Business Media LLC
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