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Label-free quantitative proteomic analysis of acquired herceptin resistance in gastric cancer cells
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Wen-hu LIU1, 3, Yi WANG3, Sheng-mao LI1, Jian-wu ZHANG1, Jin-xia CHANG2, *
Acta Pharmaceutica Sinica | 2018, 53(4) : 553 - 560
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Acta Pharmaceutica Sinica | 2018, 53(4): 553-560
ORIGINAL ARTICLES·Pharmacology
Label-free quantitative proteomic analysis of acquired herceptin resistance in gastric cancer cells
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Wen-hu LIU1, 3, Yi WANG3, Sheng-mao LI1, Jian-wu ZHANG1, Jin-xia CHANG2, *
Affiliations
  • 1. Department of Pharmacology, North Sichuan Medical College, Nanchong 637007, China
  • 2. School of Basic Medical Sciences, North Sichuan Medical College, Nanchong 637007, China
  • 3. State Key Laboratory of Proteomics, National Center for Protein Sciences, Beijing 102206, China
Published: 2018-04-12 doi: 10.16438/j.0513-4870.2017-1277
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This study was designed to explore proteins differentially expressed in HER2 positive gastric cancer N87 cells and N87/R cells with an acquired resistance to herceptin based on label-free quantitative proteomics. The extracted proteins were reduced and alkylated, then digested using filter aided sample preparation (FASP); peptides were separated via small manual reversed phase column, analyzed by LC-MS/MS, and identified with protein database 2.1 search engine. Proteins were quantified by intensity based quantification (IBQ) to search for differential proteins by comparison with relatively quantified proteins. The enrichment and network construction in gene ontology (GO) terms, genes-disease and Wikipathway of differential proteins were established through Web Gestalt. A total of 8 509 proteins were detected, among them, 7 163 proteins were further analyzed by bioinformatics, of which 110 proteins were up-regulated and 70 were down-regulated in N87/R cells. The differential proteins showed a significant difference in cellular component, biological process and molecular function in GO terms, respectively. Genes-disease network analysis indicated the association of these differential proteins with neoplasm metastasis, neoplasm invasiveness and inflammation, etc. Wikipathway enrichment analysis revealed the relevance of several signaling pathways to herceptin resistance, which included IL-2, MAPK/ERK, mTOR, aurora A, Ret, NF-κB, immune-regulatory and metabolic pathway. Western blot showed a significant increase of ERK1/2 activities in N87/R cells compared with N87 cells. Correspondingly, SCH772984, a MAPK/ERK inhibitor, preferentially reduced the viability of N87/R cells. Taken together, our data suggested that the MAPK/ERK signaling pathway is one of the key pathways that mediate herceptin resistance. This study provides the basic information for exploring the mechanisms of acquired resistance to herceptin in gastric cancer cells.

herceptin  /  acquired resistance  /  proteomics  /  MAPK/ERK signaling pathway
Wen-hu LIU, Yi WANG, Sheng-mao LI, Jian-wu ZHANG, Jin-xia CHANG. Label-free quantitative proteomic analysis of acquired herceptin resistance in gastric cancer cells[J]. Acta Pharmaceutica Sinica, 2018 , 53 (4) : 553 -560 . DOI: 10.16438/j.0513-4870.2017-1277
Year 2018 volume 53 Issue 4
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Article Info
doi: 10.16438/j.0513-4870.2017-1277
  • Receive Date:2017-12-21
  • Online Date:2026-01-15
  • Published:2018-04-12
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History
  • Received:2017-12-21
  • Revised:2018-01-19
Funding
Affiliations
    1. Department of Pharmacology, North Sichuan Medical College, Nanchong 637007, China
    2. School of Basic Medical Sciences, North Sichuan Medical College, Nanchong 637007, China
    3. State Key Laboratory of Proteomics, National Center for Protein Sciences, Beijing 102206, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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