Articles related to melanoma
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March 14, 2014 at 2:55 pm #21870
Violeta
ParticipantJust for our info: ”Differential influence of vemurafenib and dabrafenib on patients’ lymphocytes despite similar clinical efficacy in melanoma”
http://annonc.oxfordjournals.org/content/25/3/747 ‘
‘{…}While both compounds have comparable clinical efficacy, vemurafenib but not dabrafenib decreases patients peripheral lymphocyte counts and alters CD4+ T cell phenotype and function. Thus, selective BRAFi can significantly affect patients’ peripheral lymphocyte populations. Fully understanding these effects could be critical for successfully implementing combinatorial therapies of BRAFi with immunomodulatory agents.March 14, 2014 at 3:16 pm #63807Violeta
ParticipantI was thinking that it will be useful to post here articles or interesting research on melanoma. Me for example, I am reading almost everything I have access to.. and I am interested in more.I am sure a lot of you are doing the same.
Thus, if you agree and find as well articles on melanoma to share, maybe it is nice have them in one place..
Violeta
March 27, 2014 at 9:56 pm #63808Violeta
ParticipantRecent published article: although not very easy to understand the article contain information about how tumor resistance became reversible (patients respond again) with a drug holiday regime of Braf inhibitors (zelboraf for example). ”Reversible and adaptive resistance to BRAF(V600E) inhibition in melanoma”
http://www.nature.com/nature/journal/vaop/ncurrent/full/nature13121.html In a heterogeneous population of melanoma cells having varying levels of SOX10 suppression, cells with low SOX10 and consequently high EGFR expression are rapidly enriched in the presence of drug, but this is reversed when the drug treatment is discontinued. We find evidence for SOX10 loss and/or activation of TGF-β signalling in 4 of the 6 EGFR-positive drug-resistant melanoma patient samples. Our findings provide a rationale for why some BRAF or MEK inhibitor-resistant melanoma patients may regain sensitivity to these drugs after a ‘drug holiday’ and identify patients with EGFR-positive melanoma as a group that may benefit from re-treatment after a drug holiday.If somebody has access to full article please let me know, I am curious to read it.April 11, 2014 at 9:22 am #63809Violeta
ParticipantThrough a friend I discovered yesterday an interesting article about the effect of copper on melanoma tumors: http://www.nature.com/nature/journal/vaop/ncurrent/full/nature13180.html#access ‘
‘Cu chelators used in the treatment of Wilson disease decreased tumour growth of human or murine cells transformed by BRAFV600E or engineered to be resistant to BRAF inhibition. Taken together, these results suggest that Cu-chelation therapy could be repurposed to treat cancers containing the BRAFV600E mutation”Linked to this I noticed also a pilot study combining trientina (a cooper chelator) and vemurafenib.
http://clinicaltrials.gov/ct2/show/NCT02068079 I hope something good will come out from this study.
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