Literature DB >> 19192642

VEGF-1 expression in colorectal cancer is associated with disease localization, stage, and long-term disease-specific survival.

Riyad Bendardaf1, Abdelbaset Buhmeida, Marja Hilska, Matti Laato, Stina Syrjänen, Kari Syrjänen, Yrjö Collan, Seppo Pyrhönen.   

Abstract

BACKGROUND: Angiogenesis plays an important role in progression of colorectal carcinoma (CRC). Evidence from preclinical and clinical studies indicates that vascular endothelial growth factor (VEGF) is the predominant angiogenic factor in CRC. Indeed, VEGF is expressed in approximately 50% of CRCs, with minimal to no expression in normal colonic mucosa and adenomas. In this study, the expression of VEGF-1 was examined in stage I-IV CRCs to determine its clinicopathological correlates, and association with the response to treatment and disease outcome. PATIENTS AND METHODS: The present series consisted of tissue samples obtained from 360 patients with stage I, II, III, or IV CRC who had undergone large bowel resection during 1981-1990 at Turku University Hospital. Archival paraffin-embedded CRC tissue samples were used to build up tissue microarray (TMA) blocks and VEGF-1 expression was assessed immunohistochemically using an automated staining system. Three different grading systems were applied to evaluate the expression of VEGF-1.
RESULTS: Seventy percent of patients with stage IV CRC had positive VEGF-1 expression, while 50% and 47%, respectively of patients with stage II and III CRC had positive VEGF-1 expression (p = 0.005). VEGF-1 expression in the left colon and rectum was significantly higher than that in the right colon (61% vs. 45%, respectively) (p = 0.006). Significant statistical correlation (p = 0.04) was found between VEGF-1 and 10-year disease-specific survival: patients who died of the disease more frequently had a VEGF-1-expressing tumour than did those who survived for 10 years.
CONCLUSION: Quantification of VEGF-1 expression seems to provide valuable prognostic information in CRC, particularly in selecting those patients at high risk for disease progression who are likely to benefit from adjuvant therapy.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 19192642

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  38 in total

1.  Immune response gene expression in colorectal cancer carries distinct prognostic implications according to tissue, stage and site: a prospective retrospective translational study in the context of a hellenic cooperative oncology group randomised trial.

Authors:  George Pentheroudakis; Georgia Raptou; Vassiliki Kotoula; Ralph M Wirtz; Eleni Vrettou; Vasilios Karavasilis; Georgia Gourgioti; Chryssa Gakou; Konstantinos N Syrigos; Evangelos Bournakis; Grigorios Rallis; Ioannis Varthalitis; Eleni Galani; Georgios Lazaridis; George Papaxoinis; Dimitrios Pectasides; Gerasimos Aravantinos; Thomas Makatsoris; Konstantine T Kalogeras; George Fountzilas
Journal:  PLoS One       Date:  2015-05-13       Impact factor: 3.240

2.  Intestinal protein expression profile identifies inflammatory bowel disease and predicts relapse.

Authors:  Jun Shen; Yuqi Qiao; Zhihua Ran; Tianrong Wang; Jiangtao Xu; Jinsun Feng
Journal:  Int J Clin Exp Pathol       Date:  2013-04-15

3.  Liposomal prednisolone phosphate potentiates the antitumor activity of liposomal 5-fluorouracil in C26 murine colon carcinoma in vivo.

Authors:  Laura Patras; Bianca Sylvester; Lavinia Luput; Alina Sesarman; Emilia Licarete; Alina Porfire; Dana Muntean; Denise Minerva Drotar; Alexandra Doina Rusu; Andras-Laszlo Nagy; Cornel Catoi; Ioan Tomuta; Laurian Vlase; Manuela Banciu; Marcela Achim
Journal:  Cancer Biol Ther       Date:  2017-07-11       Impact factor: 4.742

4.  Genetic variants within obesity-related genes are associated with tumor recurrence in patients with stages II/III colon cancer.

Authors:  Ana Sebio; Armin Gerger; Satoshi Matsusaka; Dongyun Yang; Wu Zhang; Stefan Stremitzer; Sebastian Stintzing; Yu Sunakawa; Shinichi Yamauchi; Yan Ning; Yoshiya Fujimoto; Masashi Ueno; Heinz-Josef Lenz
Journal:  Pharmacogenet Genomics       Date:  2015-01       Impact factor: 2.089

5.  Tumor suppressors miR-143 and miR-145 and predicted target proteins API5, ERK5, K-RAS, and IRS-1 are differentially expressed in proximal and distal colon.

Authors:  Joel Pekow; Katherine Meckel; Urszula Dougherty; Fatma Butun; Reba Mustafi; John Lim; Charis Crofton; Xindi Chen; Loren Joseph; Marc Bissonnette
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2014-12-04       Impact factor: 4.052

6.  The DEAD box protein p68: a novel coactivator of Stat3 in mediating oncogenesis.

Authors:  M Sarkar; V Khare; M K Ghosh
Journal:  Oncogene       Date:  2016-12-12       Impact factor: 9.867

7.  Effect of PI3K gene silencing on growth, migration and related proteins expression of CD40 signal-mediated gastric cancer cells.

Authors:  Rui Li; Wei-Chang Chen; Xue-Qin Pang; Wen-Yan Tian; Wei-Peng Wang; Xue Guang Zhang
Journal:  Mol Biol Rep       Date:  2012-11-01       Impact factor: 2.316

Review 8.  A conceptual model of social networks and mechanisms of cancer mortality, and potential strategies to improve survival.

Authors:  Candyce H Kroenke
Journal:  Transl Behav Med       Date:  2018-07-17       Impact factor: 3.046

9.  Association of Primary Tumor Site With Mortality in Patients Receiving Bevacizumab and Cetuximab for Metastatic Colorectal Cancer.

Authors:  Mayada A Aljehani; John W Morgan; Laurel A Guthrie; Brice Jabo; Majed Ramadan; Khaled Bahjri; Sharon S Lum; Matthew Selleck; Mark E Reeves; Carlos Garberoglio; Maheswari Senthil
Journal:  JAMA Surg       Date:  2018-01-01       Impact factor: 14.766

10.  Correlation between vascular endothelial growth factor-A expression and tumor location and invasion in patients with colorectal cancer.

Authors:  Susanna Hilda Hutajulu; Dewi Kartikawati Paramita; Joyo Santoso; Muhammad Ivan Aulia Sani; Aghnia Amalia; Gatri Wulandari; Ahmad Ghozali; Johan Kurnianda
Journal:  J Gastrointest Oncol       Date:  2018-12
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.