New Anti-tumor compounds from Curcumin
Curcumin is known to have many anti-tumor such as tumor growth inhibition and induction apotosis. However, the limited bioavailability of curcumin prevented clinical application. A synthesized curcumin analogues, 1,5-diaryl-3-oxo-1 ,4-pentadiene as GO-Y030, has the potential for increased anti-tumor in vitro and in mouse models of colorectal carcinogenesis.
From the results of tests on mice, they found a survival rate of mice given the compounds synthesized. The conclusions of their research are:
The 1,5-diaryl-3-oxo-1 ,4-pentadiene analogs can yield good lead compounds for cancer chemotherapy, to Overcome the low bioavailability of curcumin.
For the full article on this research. You can read it at the following link;
http://www.biomedcentral.com/1471-2210/11/4
The History of Breast Cancer
In the 1970's the movement to increase breast cancer awareness began to grow rapidly. More and more non-profit organizations, governmental organizations and other organizations have been formed in order to increase knowledge and awareness of this disease, but also to sponsor research to aid in its eradication. While breast cancer survival rates have gone up somewhat in the last twenty years, the fact remains that this disease is still far too prevalent and killing far too many women.
Review of: Tumour invasion and metastasis initiated by microRNA-10b in breast cancer
Breast Cancer Online (2008), 11:e2 Cambridge University Press
Copyright © Cambridge University Press 2008
doi:10.1017/S1470903108006688
Alex Swarbricka1 c1
a1 Cancer Research Program, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia
Abstract
Citation of the original article: L. Ma, J. Teruya-Feldstein, R. A. Weinberg. Nature 2007; 449(7163): 682–688; Epub 26 September 2007.
Abstract of the original article: MicroRNAs have been implicated in regulating diverse cellular pathways. Although there is emerging evidence that some microRNAs can function as oncogenes or tumour suppressors, the role of microRNAs in mediating cancer metastasis remains unexplored. Here we show, using a combination of mouse and human cells, that microRNA-10b (miR-10b) is highly expressed in metastatic breast cancer cells and positively regulates cell migration and invasion. Overexpression of miR-10b in otherwise non-metastatic breast tumours initiates robust invasion and metastasis. Expression of miR-10b is induced by the transcription factor Twist, which binds directly to the putative promoter of miR-10b (MIRN10B). The miR-10b induced by Twist proceeds to inhibit translation of the messenger RNA encoding homeobox D10, resulting in increased expression of a well-characterized pro-metastatic gene, RhoC. Significantly, the level of miR-10b expression in primary breast carcinomas correlates with clinical progression. These findings suggest the workings of an undescribed regulatory pathway, in which a pleiotropic transcription factor induces expression of a specific microRNA, which suppresses its direct target and in turn activates another pro-metastatic gene, leading to tumour cell invasion and metastasis.
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