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ITRAQ-based Quantitative Proteomics Analysis of protein profile response to Pink1 deletion in breast cancer

ABSTRACT: ITRAQ technique was applied to compare the comprehensive protein expression profiles between MDA-MB-231con and MDA-MB-231Pink1-/- cells, and the original mass spectrum data were searched using Mascot engine against the UniProt database and the decoy database. Proteins were identified to be significantly according to the cut-off of a fold change ≥1.2 or ≤0.83 and a P-value ＜0.05. All of the pathways and GO enrichment analyses were performed to identify the critical proteins induced by Pink1 deletion.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (human)

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

DISEASE(S): Breast Cancer

SUBMITTER: Liqin Li

LAB HEAD: LiQin Li

PROVIDER: PXD027405 | Pride | 2023-03-11

REPOSITORIES: Pride

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Publications

Pink1 promotes cell proliferation and affects glycolysis in breast cancer.

Li Jing J Xu Xuting X Huang Huilian H Li Liqin L Chen Jing J Ding Yunfeng Y Ping Jinliang J

Experimental biology and medicine (Maywood, N.J.) 20220411 12

Phosphatase and tensin homolog (PTEN)-induced kinase 1 (Pink1) is regarded as a tumor suppressor and plays an important role in cancer cell biology, while relatively few studies have examined Pink1 in breast cancer, especially in vivo. The aims of this study were to investigate Pink1 expression in different subtypes of breast cancer tissues and cell lines and explore the effect of Pink1 protein on breast cancer. In these experiments, Pink1 expression was ...[more]

PMID: 35410525

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Expression data of control-shRNA and SATB1-shRNA expressing MDA-MB-231 cells from 2D and 3D culture system

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