Proteomics

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OC-MS/MS - HSP60-regulated Mitochondrial Proteostasis and Protein Translation Promote Tumor Growth of Ovarian Cancer


ABSTRACT: Ovarian cancer (OC) is the most lethal gynecological carcinoma because of the lack of early diagnostic markers and effective drug targets. Discovery of new therapeutic targets in OC to improve the treatment outcome is urgently needed. Patients with recurrent EOC after initial therapy have few treatment options that greatly compromises their quality of life and life expectancy. Discovery of new therapeutic targets in EOC to improve the treatment outcome is urgently needed. Proteomic analysis is one of the approaches to identify therapeutic targets in OC.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Epithelial Ovarian Cancer Cell

SUBMITTER: Jianying Guo  

LAB HEAD: Haiteng Deng

PROVIDER: PXD013811 | Pride | 2019-09-09

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
MS170626_A2780_0506_1_1.raw Raw
MS170626_A2780_0506_1_10.raw Raw
MS170626_A2780_0506_1_11.raw Raw
MS170626_A2780_0506_1_12.raw Raw
MS170626_A2780_0506_1_2.raw Raw
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Publications

HSP60-regulated Mitochondrial Proteostasis and Protein Translation Promote Tumor Growth of Ovarian Cancer.

Guo Jianying J   Li Xiao X   Zhang Wenhao W   Chen Yuling Y   Zhu Songbiao S   Chen Liang L   Xu Renhua R   Lv Yang Y   Wu Di D   Guo Mingzhou M   Liu Xiaohui X   Lu Weiguo W   Deng Haiteng H  

Scientific reports 20190902 1


Ovarian cancer (OC) is the most lethal gynecological carcinoma due to the lack of diagnostic markers and effective drug targets. Discovery of new therapeutic targets in OC to improve the treatment outcome is urgently needed. We performed proteomic analysis of OC specimens and the paired normal tissues and revealed that proteins associated with mitochondrial proteostasis and protein translation were highly expressed in ovarian tumor tissues, indicating that mitochondria are required for tumor pro  ...[more]

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