English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Background The mechanistic target of rapamycin (mTOR) is a central regulator of cell growth and proliferation, and its aberrant activation is frequent in cancer [1]. We have previously shown that sterol regulatory element binding protein (SREBP) is a major transcriptional effector of mTOR complex 1 (mTORC1) signaling [2]. SREBP is a transcription factor that stimulates the expression of genes involved in the de novo synthesis of lipids [3]. Since mTORC1 is commonly activated in cancer through upstream oncogenic signaling pathways and enhanced lipogenesis is a metabolic hallmark of tumor cells, we hypothesize that the mTORC1-SREBP pathway is important for tumor metabolism and growth.

Oncogenic signaling upstream of mTORC1 drives lipogenesis and proliferation through SREBP