2021
DOI: 10.7150/jca.63517
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Decipher the Helicobacter pylori Protein Targeting in the Nucleus of Host Cell and their Implications in Gallbladder Cancer: An insilico approach

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Cited by 16 publications
(8 citation statements)
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“…Therefore, novel immunotherapy strategies are urgently needed for the majority of patients with mCRC. With the advancement of molecular techniques, next‐generation sequencing (NGS) analyses focused on novel approaches for the characterization and identification of microbial communities, which play an important role in different diseases and cancers such as colon cancer, cervical cancer, prostate cancer, lung cancer and gallbladder cancer 5‐10 …”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Therefore, novel immunotherapy strategies are urgently needed for the majority of patients with mCRC. With the advancement of molecular techniques, next‐generation sequencing (NGS) analyses focused on novel approaches for the characterization and identification of microbial communities, which play an important role in different diseases and cancers such as colon cancer, cervical cancer, prostate cancer, lung cancer and gallbladder cancer 5‐10 …”
Section: Introductionmentioning
confidence: 99%
“…With the advancement of molecular techniques, nextgeneration sequencing (NGS) analyses focused on novel approaches for the characterization and identification of microbial communities, which play an important role in different diseases and cancers such as colon cancer, cervical cancer, prostate cancer, lung cancer and gallbladder cancer. [5][6][7][8][9][10] We have recently reported the results of Cetuximab-AVElumab-mCRC (CAVE-mCRC), a single-arm, phase II trial, in which the combination of cetuximab, an anti-epidermal growth factor receptor (EGFR) monoclonal antibody (mAb) plus avelumab, an antiprogrammed death ligand 1 (PD-L1) mAb, was evaluated as rechallenge strategy in chemo-refractory RAS wild type (WT) mCRC patients. 11 The rationale for this combination is based on the induction of antibody-dependent cell-mediated cytotoxicity (ADCC) by these two IgG isotype mAbs, which could enhance Natural Killer (NK) cell-mediated antitumor immune response.…”
Section: Introductionmentioning
confidence: 99%
“…H. pylori can inhibit the expression of p53 protein and normal cellular transformation by expressing multiple effectors targeting the host nucleus, which in turn leads to GBC progression ( Arana and Kunkel, 2010 ; Wei et al., 2010 ). Its effectors include DNA topoisomerase, DNA polymerase III, bacterial insertion sequence 200 or 607 (IS200 or IS607), translation initiation factor-3 (IF-3), ribosome-recycling factor (RRF), 30S ribosomal protein S8 and various uncharacterized proteins ( Wang et al., 2021b ). DNA topoisomerase, DNA polymerase III, IS200 and IS607 cause genomic instability in infected cells by interfering with the process of gene replication ( Bao and Jurka, 2013 ; Subramaniam et al., 2014 ).…”
Section: Bacteria In Gbc Pathogenesismentioning
confidence: 99%
“…DNA topoisomerase, DNA polymerase III, IS200 and IS607 cause genomic instability in infected cells by interfering with the process of gene replication ( Bao and Jurka, 2013 ; Subramaniam et al., 2014 ). Among them, IS200 and IS607 encode a transposase (TnpA) and a protein (TnpB), respectively, thought to be methyltransferases ( Wang et al., 2021b ). Conversely, IF-3, RRF and 30S ribosomal protein S8 can disrupt protein synthesis by altering the transcription and translation processes of genes.…”
Section: Bacteria In Gbc Pathogenesismentioning
confidence: 99%
“…A recent study by Wang et al [60] identified H. pylori proteins with potential involvement in gallbladder cancer pathogenesis using a bioinformatics approach. Briefly, the UniProt database containing the entire H. pylori proteome was used to predict which H. pylori proteins may potentially target the nucleus of host cells.…”
Section: Biliary Tract Cancersmentioning
confidence: 99%