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• W2059246376 startingPage "1" @default.
• W2059246376 abstract "Multiple genetic abnormalities will have occurred in advanced cervical cancer and multiple targeting is likely to be needed to control tumor growth. To date, dominant therapeutic targets under scrutiny for cervical cancer treatment have been EGFR pathway and angiogenesis inhibition as well as anti-HPV vaccines. The potentially most effective targets to be blocked may be downstream from the membrane receptor or at the level of the nucleus. Alterations of the pathways involved in DNA repair and in checkpoint activations, as well as the specific site of HPV genome integration, appear worth assessing. For genetic mutational analysis, complete exon sequencing may become the norm in the future but at this stage frequent mutations (that matter) can be verified by PCR analysis. A precise documentation of relevant alterations of a large spectrum of protein biomarkers can be carried out by reverse phase protein array (RPPA) or by multiplex analysis. Clinical decision-making on the drug(s) of choice as a function of the biological alteration will need input from bio-informatics platforms as well as novel statistical designs. Endpoints are yet to be defined such as the loss (or reappearance) of a predictive biomarker. Single or dual targeting needs to be explored first in relevant preclinical animal and in xenograft models prior to clinical deployment." @default.
• W2059246376 created "2016-06-24" @default.
• W2059246376 creator A5007994675 @default.
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• W2059246376 creator A5085925712 @default.
• W2059246376 creator A5090489400 @default.
• W2059246376 date "2011-07-06" @default.
• W2059246376 modified "2023-10-18" @default.
• W2059246376 title "Pathway Profiling and Rational Trial Design for Studies in Advanced Stage Cervical Carcinoma: A Review and a Perspective" @default.
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• W2059246376 doi "https://doi.org/10.5402/2011/403098" @default.
• W2059246376 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3195803" @default.

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