Proteomics

Dataset Information

0

Circulating SOD2 is a Response Biomarker for Neoadjuvant Therapy in Breast Cancer


ABSTRACT: There is a great need of non-invasive tools that inform of an early molecular response to cancer therapeutic treatment. Here, we have tested the hypothesis that proteolytically resistant proteins could be candidate circulating tumor biomarkers for cancer therapy. Proteins resistant to proteolysis are drastically under-sampled by current proteomic workflows. These proteins could be reliable sensors for the response to therapy since they are likely to stay longer in circulation. We selected Manganese superoxide dismutase (SOD2), a mitochondrial redox enzyme, from a screening of proteolytic resistant proteins in breast cancer (BC). First, we confirmed the robustness of SOD2 and determined that its proteolytic resistance is mediated by its quaternary protein structure. We also proved that the release of SOD2 upon chemotherapy treatment correlates with cell death in BC cells. Then, after confirming that SOD2 is very stable in human serum, we sought to measure its circulating levels in a cohort of BC patients undergoing neoadjuvant therapy. The results showed that circulating levels of SOD2 increased when patients respond to the treatment according to the tumor shrinkage during neoadjuvant chemotherapy. Therefore, the measurement of SOD2 levels in plasma could improve the non-invasive monitoring of the therapeutic treatment in breast cancer patients. The identification of circulating biomarkers linked to the tumor cell death induced by treatment could be a useful for monitoring the action of the large number of cancer drugs currently used in the clinic. We envision that our approach could help uncover candidate tumor biomarkers to measure a tumor’s response to cancer therapy in real time by sampling the tumor throughout the course of treatment.

INSTRUMENT(S): LTQ Orbitrap Velos

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Epithelial Cell, Cell Culture

DISEASE(S): Breast Cancer

SUBMITTER: Francesc Canals  

LAB HEAD: Josep Villanueva

PROVIDER: PXD032359 | Pride | 2023-01-09

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
BT549-Control_GnHCl_01.dat Other
BT549-Control_GnHCl_01.mgf Mgf
BT549-Control_GnHCl_01.raw Raw
BT549-Control_GnHCl_02.dat Other
BT549-Control_GnHCl_02.mgf Mgf
Items per page:
1 - 5 of 37
altmetric image

Publications


There is a great need for non-invasive tools that inform of an early molecular response to cancer therapeutic treatment. Here, we tested the hypothesis that proteolytically resistant proteins could be candidate circulating tumor biomarkers for cancer therapy. Proteins resistant to proteolysis are drastically under-sampled by current proteomic workflows. These proteins could be reliable sensors for the response to therapy since they are likely to stay longer in circulation. We selected manganese  ...[more]

Similar Datasets

2013-07-20 | E-GEOD-49035 | biostudies-arrayexpress
2023-03-11 | PXD038553 | Pride
2023-06-30 | E-MTAB-12828 | biostudies-arrayexpress
2011-03-01 | E-GEOD-23720 | biostudies-arrayexpress
2014-09-22 | E-GEOD-51372 | biostudies-arrayexpress
2021-02-09 | PXD014328 | Pride
2013-07-20 | GSE49035 | GEO
2018-10-19 | PXD009570 | Pride
2015-05-08 | E-GEOD-68651 | biostudies-arrayexpress
2019-12-03 | E-MTAB-8055 | biostudies-arrayexpress