Proteomics

Dataset Information

0

Quantitative proteomics of TNBC


ABSTRACT: Quantitative proteomics of triple negative breast cancer patient derived cell lines.

INSTRUMENT(S): TripleTOF 5600

ORGANISM(S): Homo Sapiens (human)

SUBMITTER: René Zahedi  

LAB HEAD: Rene Zahedi

PROVIDER: PXD013872 | Pride | 2019-11-25

REPOSITORIES: Pride

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Publications

A Unique Morphological Phenotype in Chemoresistant Triple-Negative Breast Cancer Reveals Metabolic Reprogramming and PLIN4 Expression as a Molecular Vulnerability.

Sirois Isabelle I   Aguilar-Mahecha Adriana A   Lafleur Josiane J   Fowler Emma E   Vu Viet V   Scriver Michelle M   Buchanan Marguerite M   Chabot Catherine C   Ramanathan Aparna A   Balachandran Banujan B   Légaré Stéphanie S   Przybytkowski Ewa E   Lan Cathy C   Krzemien Urszula U   Cavallone Luca L   Aleynikova Olga O   Ferrario Cristiano C   Guilbert Marie-Christine MC   Benlimame Naciba N   Saad Amine A   Alaoui-Jamali Moulay M   Saragovi Horace Uri HU   Josephy Sylvia S   O'Flanagan Ciara C   Hursting Stephen D SD   Richard Vincent R VR   Zahedi René P RP   Borchers Christoph H CH   Bareke Eric E   Nabavi Sheida S   Tonellato Peter P   Roy Josée-Anne JA   Robidoux André A   Marcus Elizabeth A EA   Mihalcioiu Catalin C   Majewski Jacek J   Basik Mark M  

Molecular cancer research : MCR 20190919 12


The major obstacle in successfully treating triple-negative breast cancer (TNBC) is resistance to cytotoxic chemotherapy, the mainstay of treatment in this disease. Previous preclinical models of chemoresistance in TNBC have suffered from a lack of clinical relevance. Using a single high dose chemotherapy treatment, we developed a novel MDA-MB-436 cell-based model of chemoresistance characterized by a unique and complex morphologic phenotype, which consists of polyploid giant cancer cells giving  ...[more]

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