Proteomics

Dataset Information

0

Stress hormones induce breast intra-tumor heterogeneity


ABSTRACT: Diversity within or between a tumour and metastases, known as intra-patient tumour heterogeneity develops during disease progression, and is a serious hurdle for therapy1,2,3. Metastasis is the fatal hallmark of cancer and mechanisms of colonization, the most complex step of the metastatic cascade4,5, remain ill-defined. Better understanding of cellular and molecular processes underlying intra-patient tumour heterogeneity and metastasis are pivotal for the success of personalized cancer treatment. Here, transcriptional profiling of tumours and matched metastases showed cancer site-specific phenotypes, and identified increased glucocorticoid receptor (GR) activity in the distant metastases. GR has been shown to mediate the effects of stress hormones and of their synthetic derivatives, widely used in the clinic as anti-inflammatory and immunosuppressive.

OTHER RELATED OMICS DATASETS IN: GSE124817

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Permanent Cell Line Cell, Cell Culture

DISEASE(S): Breast Cancer

SUBMITTER: Alexander Schmidt  

LAB HEAD: Alexander Schmidt

PROVIDER: PXD009102 | Pride | 2019-03-25

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
001_PO4-1_C17.raw Raw
001_TMT-1_C17.mgf Mgf
001_TMT-1_C17.pride.mgf.gz Mgf
001_TMT-1_C17.raw Raw
002_PO4-1_C17.raw Raw
Items per page:
1 - 5 of 50
altmetric image

Publications


Diversity within or between tumours and metastases (known as intra-patient tumour heterogeneity) that develops during disease progression is a serious hurdle for therapy<sup>1-3</sup>. Metastasis is the fatal hallmark of cancer and the mechanisms of colonization, the most complex step in the metastatic cascade<sup>4</sup>, remain poorly defined. A clearer understanding of the cellular and molecular processes that underlie both intra-patient tumour heterogeneity and metastasis is crucial for the  ...[more]

Similar Datasets

2021-09-12 | GSE176029 | GEO
2013-11-11 | E-GEOD-46826 | biostudies-arrayexpress
2016-07-11 | GSE63490 | GEO
2023-02-17 | PXD039409 | Pride
2023-03-11 | PXD036434 | Pride
2011-08-06 | GSE31232 | GEO
2011-08-25 | GSE31610 | GEO
2011-08-24 | E-GEOD-31610 | biostudies-arrayexpress
2011-08-05 | E-GEOD-31232 | biostudies-arrayexpress
2013-11-11 | GSE46826 | GEO