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Prognosis value of heat-shock proteins in esophageal and esophagogastric cancer: A systematic review and meta-analysis.
Nakamura, Eric Toshiyuki; Park, Amanda; Pereira, Marina Alessandra; Kikawa, Daniel; Tustumi, Francisco.
Afiliação
  • Nakamura ET; Department of Gastroenterology, Instituto do Câncer, Hospital das Clínicas da Universidade de São Paulo, Faculdade de Medicina, Universidade de São Paulo, São Paulo 01246000, Brazil.
  • Park A; Department of Scientific Initiation, Universidade Mogi das Cruzes, São Paulo 08780911, Brazil.
  • Pereira MA; Department of Evidence-Based Medicine, Centro Universitário Lusíada, Centre for Evidence-Based Medicine, Centro Universitário Lusíada (UNILUS), Santos, Brazil.
  • Kikawa D; Department of Gastroenterology, Instituto do Câncer, Hospital das Clínicas da Universidade de São Paulo, Faculdade de Medicina, Universidade de São Paulo, São Paulo 01246000, Brazil.
  • Tustumi F; Department of Scientific Initiation, Universidade Mogi das Cruzes, São Paulo 08780911, Brazil.
World J Gastrointest Oncol ; 16(4): 1578-1595, 2024 Apr 15.
Article em En | MEDLINE | ID: mdl-38660660
ABSTRACT

BACKGROUND:

Heat shock proteins (HSPs) are molecular chaperones that play an important role in cellular protection against stress events and have been reported to be overexpressed in many cancers. The prognostic significance of HSPs and their regulatory factors, such as heat shock factor 1 (HSF1) and CHIP, are poorly understood.

AIM:

To investigate the relationship between HSP expression and prognosis in esophageal and esophagogastric cancer.

METHODS:

A systematic review was conducted in accordance with PRISMA recommendations (PROSPERO CRD42022370653), on Embase, PubMed, Cochrane, and LILACS. Cohort, case-control, and cross-sectional studies of patients with esophagus or esophagogastric cancer were included. HSP-positive patients were compared with HSP-negative, and the endpoints analyzed were lymph node metastasis, tumor depth, distant metastasis, and overall survival (OS). HSPs were stratified according to the HSP family, and the summary risk difference (RD) was calculated using a random-effect model.

RESULTS:

The final selection comprised 27 studies, including esophageal squamous cell carcinoma (21), esophagogastric adenocarcinoma (5), and mixed neoplasms (1). The pooled sample size was 3465 patients. HSP40 and 60 were associated with a higher 3-year OS [HSP40 RD = 0.22; 95% confidence interval (CI) 0.09-0.35; HSP60 RD = 0.33; 95%CI 0.17-0.50], while HSF1 was associated with a poor 3-year OS (RD = -0.22; 95%CI -0.32 to -0.12). The other HSP families were not associated with long-term survival. HSF1 was associated with a higher probability of lymph node metastasis (RD = -0.16; 95%CI -0.29 to -0.04). HSP40 was associated with a lower probability of lymph node dissemination (RD = 0.18; 95%CI 0.03-0.33). The expression of other HSP families was not significantly related to tumor depth and lymph node or distant metastasis.

CONCLUSION:

The expression levels of certain families of HSP, such as HSP40 and 60 and HSF1, are associated with long-term survival and lymph node dissemination in patients with esophageal and esophagogastric cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: World J Gastrointest Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: World J Gastrointest Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil