Back to search

Article

The c-KIT Exon 11 Deletions Cause Resistant to Imatinib Treatment of GISTs through Induction of ULK1-SRC related Autophagy

2020-04-10

Abstract excerpt

<h4>Background: </h4> Exon 11 deletion of c-KIT is the common mutation site with the worst prognosis of gastrointestinal stromal tumors (GISTs). Autophagy has shown to have both protumor and antitumor functions and protect GIST cells from imatinib (IM)-induced apoptosis. In this study, we aimed to explore whether c-KIT exon 11 deletions of GISTs drive refractory to IM treatment through regulation of autophagy. <h4...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
154efa8c-df2d-5172-be54-05f7657189d1
DOI
10.21203/rs.3.rs-22031/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
The c-KIT Exon 11 Deletions Cause Resistant to Imatinib Treatment of GISTs through Induction of ULK1-SRC related AutophagyDOI 10.21203/rs.3.rs-22031/v1
Select a neighboring publication to make it the new centre.