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Melanoma chemoprevention

LOX has been found to be an important marker for cancer progression within the melanoma system, and therefore could be a useful biomarker and therapeutic target for melanoma chemoprevention (Winer et al., 2002). It also has been found that 12(S)-HETE is involved in the proliferation of pancreatic carcinoma cells (Ding et al., 2001) and inhibition of the 12-LOX has been shown to cause apoptosis of these cells (Tong et ah, 2002). 12-LOX and 12(S)-HETE were also found to enhance proliferation and survival of gastric cancer cell lines (Wong et al., 2001). [Pg.155]

Halpem, A. G., Retinoids and the chemoprevention of melanoma, in Advances in the Biology and Treatment cf Cutaneous Melanoma, Meeting Abstracts, Boston, MA, November 6 and 7,1998. [Pg.87]

Finally, chemoprevention with systemic retinoids has demonstrated promise in decreasing the incidence of new primary non-melanoma skin cancers (NMSCs) in immxmocompromised post-transplantation recipients. However, there is limited evidence for the use of systemic retinoids in the non-transplantation patients at high risk for NMSC. This study was designed as prospective, randomised, double-blind, placebo-controlled clinical trial [3. ... [Pg.203]


See other pages where Melanoma chemoprevention is mentioned: [Pg.379]    [Pg.113]    [Pg.167]    [Pg.91]    [Pg.176]    [Pg.113]    [Pg.128]    [Pg.19]    [Pg.310]    [Pg.311]    [Pg.15]    [Pg.225]    [Pg.1932]    [Pg.2223]    [Pg.171]    [Pg.141]    [Pg.221]   
See also in sourсe #XX -- [ Pg.155 ]




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