Proteomics

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Phosphoproteomics Profiling of Non-Small Cell Lung Cancer Cells Treated with a Novel Phosphatase Activator


ABSTRACT: Activation of protein phosphatase 2A (PP2A) is a promising anti-cancer therapeutic strategy given this tumor suppressor’s ability to coordinately downregulate multiple pathways involved with growth and proliferation.Here, we studied the global signaling response signature of a novel small molecule activator of PP2A (SMAP). Through an exploration of the global phosphoproteomicalterations of two KRAS mutated non-small cell lung cancer (NSCLC) cell lines (A549 and H358)in the context of PP2A activation, we sought to identify the pathway-level perturbations and uncover candidate proteins that are potentially key targets of SMAP regulation.

INSTRUMENT(S): LTQ Orbitrap Elite

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Lung, Permanent Cell Line Cell

DISEASE(S): Bronchiolo-alveolar Adenocarcinoma

SUBMITTER: Danica Wiredja  

LAB HEAD: Mark R. Chance

PROVIDER: PXD005698 | Pride | 2018-07-05

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
C1_A_H358 CAP-40-2156.pride.mgf.gz Mgf
C1_A_H358CAP-40-2156.mgf Mgf
C1_A_H358CAP-40-2156.raw Raw
C1_B_H358 CAP-40-2158.pride.mgf.gz Mgf
C1_B_H358CAP-40-2158.mgf Mgf
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Publications

Phosphoproteomics Profiling of Nonsmall Cell Lung Cancer Cells Treated with a Novel Phosphatase Activator.

Wiredja Danica D DD   Ayati Marzieh M   Mazhar Sahar S   Sangodkar Jaya J   Maxwell Sean S   Schlatzer Daniela D   Narla Goutham G   Koyutürk Mehmet M   Chance Mark R MR  

Proteomics 20171025 22


Activation of protein phosphatase 2A (PP2A) is a promising anticancer therapeutic strategy, as this tumor suppressor has the ability to coordinately downregulate multiple pathways involved in the regulation of cellular growth and proliferation. In order to understand the systems-level perturbations mediated by PP2A activation, we carried out mass spectrometry-based phosphoproteomic analysis of two KRAS mutated non-small cell lung cancer (NSCLC) cell lines (A549 and H358) treated with a novel sma  ...[more]

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