gastric cancer

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New insights into the inflamed tumor immune microenvironment of gastric cancer with lymphoid stroma: from morphology and digital analysis to gene expression

Authors and Affiliations:

Irene Gullo1,2,3,4, Patrícia Oliveira3,4, Maria Athelogou5, Gilza Gonçalves2,3,4,6, Marta L Pinto4,7,8, Joana Carvalho3,4, Ana Valente3,4, Hugo Pinheiro3,4,9, Sara Andrade3,4,10, Gabriela M. Almeida3,4, Ralf Huss5, Kakoli Das11, Patrick Tan11,12,13, José C. Machado2,3,4, Carla Oliveira2,3,4, Fátima Carneiro1,2,3,4

 

New molecular mechanism to explain cases of hereditary gastric cancer

The most common cause of Hereditary Diffuse Gastric Cancer are germline mutations of the CDH1 gene. The vast majority of CDH1 germline alterations lead to truncated forms of E-cadherin with loss of protein function.

The various faces of hereditary diffuse gastric cancer

Gastric cancer: Beyond Helicobacter pylori infection

Gastric cancer is one of the most incident and deadly in the world. Helicobacter pylori infection plays a key role in the early stages of the process leading to the development of cancer. In this study, the authors show that there is a shift in the profile of the gastric microbiome from patients with chronic gastritis to patients with gastric cancer. The gastric microbiome of cancer patients is dysbiotic, presenting reduced microbial diversity, decreased abundance of H. pylori, and increased abundance of other species of bacteria.

Glicosilação de células de cancro gástrico como modulador do receptor oncogénico ErbB2

Autores e Afiliações:

Henrique O. Duarte1,2,3, Meritxell Balmaña1,2, Stefan Mereiter1,2, Hugo Osório1,2,4, Joana Gomes1,2 and Celso A. Reis1,2,3,4

1Institute for Research and Innovation in Health (i3S), University of Porto, 4200-135 Porto, Portugal

2Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), 4200-135 Porto, Portugal

Gastric Cancer Cell Glycosylation as a Modulator od the ErbB2 Oncogenic Receptor

Cell surface receptor tyrosine kinases (RTKs) play a central role in the initiation, promotion and progression of multiple human cancers, by triggering the aberrant activation of downstream signaling pathways implicated in malignant cell phenotype and behavior. In particular, overexpression of the human epidermal growth factor 2 (ErbB2) RTK constitutes a well-established molecular driver of carcinogenesis. RTK maturation is tightly regulated by protein N-linked glycosylation.

Multidisciplinary research presents new protocol for the functional characterization of missense type mutations in the gene coding for the adhesion molecule E-cadherin.

Authors and Affiliations:

Soraia Melo 1,2,3, Joana Figueiredo 1,2, Maria Sofia Fernandes 1,2,4, Margarida Gonçalves 1,5, Eurico Morais-de-Sá 1,5, João Miguel Sanches 4 and Raquel Seruca 1,2,3

1 Instituto de Investigação e Inovação em Saúde (i3S), University of Porto, 4200-135 Porto, Portugal

2 Institute of Molecular Pathology and Immunology, University of Porto (IPATIMUP), 4200-135 Porto, Portugal

Alcohol consumption and gastric cancer risk—A pooled analysis within the StoP project consortium

Porphyrin Modified Trastuzumab Improves Efficacy of HER2 Targeted Photodynamic Therapy of Gastric Cancer

A collaboration between researchers from Ipatimup/i3S, INEB/i3S and Universidade de Aveiro  led to the development of a novel photoimmunoconjugate of porphyrin conjugated to trastuzumab that specifically and efficiently eliminates HER2+ gastric cancer cells following photodynamic therapy in vitro and in vivo (when compared to trastuzumab alone).

This study suggests that, in the setting of human disease, repetitive cycles of Trast:Porph photoimmunotherapy may improve treatment of HER2+ gastric cancer patients.

 

Authors and Affiliations:

P53 deregulation in Epstein-Barr virus-associated gastric cancer


Joana Ribeiroa,b,1, Mariana Maltab,c,1, Ana Galaghard, Fernanda Silvad, Luís Pedro Afonsod, Rui Medeirosb,c,e,f, Hugo Sousab,e

1Joint first authors

a Faculty of Medicine, University of Porto, Alameda Prof. Hernani Monteiro, 4200-319 Porto, Portugal

b Molecular Oncology & Viral Pathology Group, IPO-Porto Research Center (CI-IPOP), Portugal