التفاصيل البيبلوغرافية
| العنوان: |
The constitutively active form of a key cholesterol synthesis enzyme is lipid droplet-localized and upregulated in endometrial cancer tissues. |
| المؤلفون: |
Coates, Hudson W.1, Nguyen, Tina B.1, Ximing Du1, Olzomer, Ellen M.1, Farrell, Rhonda2,3, Byrne, Frances L.1, Yang, Hongyuan1, Brown, Andrew J.1 aj.brown@unsw.edu.au |
| المصدر: |
Journal of Biological Chemistry. May2024, Vol. 300 Issue 5, p1-14. 14p. |
| مصطلحات موضوعية: |
*ENDOMETRIAL cancer, *CELL fractionation, *CANCER cell proliferation, *CHOLESTEROL, *CATALYTIC domains |
| مستخلص: |
Cholesterol is essential for both normal cell viability and cancer cell proliferation. Aberrant activity of squalene monooxygenase (SM, also known as squalene epoxidase), the ratelimiting enzyme of the committed cholesterol synthesis pathway, is accordingly implicated in a growing list of cancers. We previously reported that hypoxia triggers the truncation of SM to a constitutively active form, thus preserving sterol synthesis during oxygen shortfalls. Here, we show SM truncation is upregulated and correlates with the magnitude of hypoxia in endometrial cancer tissues, supporting the in vivo relevance of our earlier work. To further investigate the pathophysiological consequences of SM truncation, we examined its lipid dropletlocalized pool using complementary immunofluorescence and cell fractionation approaches and found that it exclusively comprises the truncated enzyme. This partitioning is facilitated by the loss of an endoplasmic reticulum-embedded region at the SM N terminus, whereas the catalytic domain containing membrane-associated C-terminal helices is spared. Moreover, we determined multiple amphipathic helices contribute to the lipid droplet localization of truncated SM. Taken together, our results expand on the striking differences between the two forms of SM and suggest upregulated truncation may contribute to SM-related oncogenesis. [ABSTRACT FROM AUTHOR] |
| قاعدة البيانات: |
Academic Search Index |
Full Text Finder