Literature DB >> 21533942

Expression of bone morphogenic protein-4 is inversely related to prevalence of lymph node metastasis in gastric adenocarcinoma.

Seong-Gon Kim1, Hye-Rim Park, Soo-Kee Min, Je-Yong Choi, Sung-Hoon Koh, Jong-Wan Kim, Hae-Wan Lee.   

Abstract

PURPOSE: Bone morphogenic proteins (BMPs) are the largest subfamily of the transforming growth factor-β superfamily. Initially characterized as factors that induce bone and cartilage formation, BMPs have been found to be critical during mesoderm formation, organogenesis, and cellular differentiation. Bone morphogenic proteins are also known to modulate the morphologic alteration, adhesion, motility, and invasion of carcinoma cells derived from several organs. However, BMP-4 expression in gastric adenocarcinoma has not yet been clarified. We conducted the present study to define the clinical significance of BMP-4 expression in gastric carcinoma.
METHODS: Using immunohistochemistry, we investigated the expression of BMP-4 in normal mucosae and gastric adenocarcinoma samples from 64 patients with gastric carcinoma.
RESULTS: The expression of BMP-4 was significantly higher in the adenocarcinoma than in the normal mucosae. Moreover, increased BMP-4 expression was associated with the presence of Helicobacter pylori infection. By contrast, the BMP-4 expression rate in gastric carcinoma was inversely related to the prevalence of lymph node metastasis and tumor invasiveness.
CONCLUSIONS: The findings of this study suggest that BMP-4 expression may be a useful prognostic factor for predicting the outcome of patients with gastric carcinoma. Continued investigation to define the pathophysiologic mechanism underlying the role of BMP-4 in gastric carcinoma is warranted.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21533942     DOI: 10.1007/s00595-010-4320-2

Source DB:  PubMed          Journal:  Surg Today        ISSN: 0941-1291            Impact factor:   2.549


  26 in total

Review 1.  Linking colorectal cancer to Wnt signaling.

Authors:  M Bienz; H Clevers
Journal:  Cell       Date:  2000-10-13       Impact factor: 41.582

2.  Sonic hedgehog promotes cell cycle progression in activated peripheral CD4(+) T lymphocytes.

Authors:  Jacqueline A Lowrey; Gareth A Stewart; Susannah Lindey; Gerard F Hoyne; Margaret J Dallman; Sarah E M Howie; Jonathan R Lamb
Journal:  J Immunol       Date:  2002-08-15       Impact factor: 5.422

3.  Linking pathways in colorectal cancer.

Authors:  Gijs R van den Brink
Journal:  Nat Genet       Date:  2004-10       Impact factor: 38.330

Review 4.  Development and differentiation of the intestinal epithelium.

Authors:  P de Santa Barbara; G R van den Brink; D J Roberts
Journal:  Cell Mol Life Sci       Date:  2003-07       Impact factor: 9.261

5.  Bone morphogenetic protein-4 is overexpressed in colonic adenocarcinomas and promotes migration and invasion of HCT116 cells.

Authors:  Haiyun Deng; Ryouji Makizumi; T S Ravikumar; Huali Dong; Wancai Yang; Weng-Lang Yang
Journal:  Exp Cell Res       Date:  2007-01-10       Impact factor: 3.905

6.  Bone morphogenetic protein-4 inhibits proliferation and induces apoptosis of multiple myeloma cells.

Authors:  O Hjertner; H Hjorth-Hansen; M Börset; C Seidel; A Waage; A Sundan
Journal:  Blood       Date:  2001-01-15       Impact factor: 22.113

Review 7.  Molecular testing of Helicobacter pylori-associated chronic gastritis and premalignant gastric lesions: clinical implications.

Authors:  A R Sepulveda
Journal:  J Clin Gastroenterol       Date:  2001 May-Jun       Impact factor: 3.062

Review 8.  Review article: Cellular markers in the gastric precancerous process.

Authors:  S F Moss
Journal:  Aliment Pharmacol Ther       Date:  1998-02       Impact factor: 8.171

9.  Bone morphogenetic protein-4 induced by NDRG2 expression inhibits MMP-9 activity in breast cancer cells.

Authors:  Soo-Kyung Shon; Aeyung Kim; Ji Young Kim; Keun Il Kim; Young Yang; Jong-Seok Lim
Journal:  Biochem Biophys Res Commun       Date:  2009-05-19       Impact factor: 3.575

10.  BMP4 signaling induces senescence and modulates the oncogenic phenotype of A549 lung adenocarcinoma cells.

Authors:  S Buckley; W Shi; B Driscoll; A Ferrario; K Anderson; D Warburton
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2003-09-05       Impact factor: 5.464

View more
  5 in total

1.  Increased Expression of Gremlin1 Promotes Proliferation and Epithelial Mesenchymal Transition in Gastric Cancer Cells and Correlates With Poor Prognosis of Patients With Gastric Cancer.

Authors:  Zhiwei Sun; Shuo Cai; Chang Liu; Yuxin Cui; Jiafu Ji; Wen G Jiang; Lin Ye
Journal:  Cancer Genomics Proteomics       Date:  2020 Jan-Feb       Impact factor: 4.069

2.  Effect of bone morphogenetic protein-2 on proliferation and apoptosis of gastric cancer cells.

Authors:  Junjie Zhang; Yanli Ge; Longe Sun; Jianchun Cao; Qiong Wu; Likun Guo; Zhirong Wang
Journal:  Int J Med Sci       Date:  2012-02-15       Impact factor: 3.738

3.  Expression of bone morphogenetic protein-2 and -7 in urinary bladder cancer predicts time to tumor recurrence.

Authors:  Bolesław Kuzaka; Marek Janiak; Krzysztof H Włodarski; Piotr Radziszewski; Paweł K Włodarski
Journal:  Arch Med Sci       Date:  2015-03-18       Impact factor: 3.318

4.  Selective targeting BMP2 and 4 in SMAD4 negative esophageal adenocarcinoma inhibits tumor growth and aggressiveness in preclinical models.

Authors:  Shulin Li; Sanne J M Hoefnagel; Matthew Read; Sybren Meijer; Mark I van Berge Henegouwen; Suzanne S Gisbertz; Elena Bonora; David S H Liu; Wayne A Phillips; Silvia Calpe; Ana C P Correia; Maria D C Sancho-Serra; Sandro Mattioli; Kausilia K Krishnadath
Journal:  Cell Oncol (Dordr)       Date:  2022-07-28       Impact factor: 7.051

5.  BMP4 Signaling Is Able to Induce an Epithelial-Mesenchymal Transition-Like Phenotype in Barrett's Esophagus and Esophageal Adenocarcinoma through Induction of SNAIL2.

Authors:  Christine Kestens; Peter D Siersema; G Johan A Offerhaus; Jantine W P M van Baal
Journal:  PLoS One       Date:  2016-05-18       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.