Unknown

Dataset Information

0

Chromosomal instability triggers cell death via local signalling through the innate immune receptor Toll.


ABSTRACT: Chromosomal instability (CIN) is a hallmark of cancer and has been implicated in cancer initiation, progression and the development of resistance to traditional cancer therapy. Here we identify a new property of CIN cells, showing that inducing CIN in proliferating Drosophila larval tissue leads to the activation of innate immune signalling in CIN cells. Manipulation of this immune pathway strongly affects the survival of CIN cells, primarily via JNK, which responds to both Toll and TNF?/Eiger. This pathway also activates Mmp1, which recruits hemocytes to the CIN tissue to provide local amplification of the immune response that is needed for effective elimination of CIN cells.

SUBMITTER: Liu D 

PROVIDER: S-EPMC4770720 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Chromosomal instability triggers cell death via local signalling through the innate immune receptor Toll.

Liu Dawei D   Shaukat Zeeshan Z   Saint Robert B RB   Gregory Stephen L SL  

Oncotarget 20151101 36


Chromosomal instability (CIN) is a hallmark of cancer and has been implicated in cancer initiation, progression and the development of resistance to traditional cancer therapy. Here we identify a new property of CIN cells, showing that inducing CIN in proliferating Drosophila larval tissue leads to the activation of innate immune signalling in CIN cells. Manipulation of this immune pathway strongly affects the survival of CIN cells, primarily via JNK, which responds to both Toll and TNFα/Eiger.  ...[more]

Similar Datasets

| S-EPMC2841715 | biostudies-literature
| S-EPMC6557118 | biostudies-literature
| S-EPMC7662148 | biostudies-literature
| S-EPMC3959197 | biostudies-literature
| S-EPMC5819576 | biostudies-literature
| S-EPMC3519935 | biostudies-literature
| S-EPMC6324559 | biostudies-literature
| S-EPMC6499517 | biostudies-literature
| S-EPMC4855268 | biostudies-other
| S-EPMC2889516 | biostudies-literature