Literature DB >> 7655739

The prevalence and clinical significance of chromogranin A and secretogranin II immunoreactivity in colorectal adenocarcinomas.

S Ferrero1, R Buffa, G Pruneri, A G Siccardi, M Pelagi, A K Lee, G Coggi, S Bosari.   

Abstract

Colorectal adenocarcinomas may display features of endocrine differentiation, shown by argyrophil stains and by the expression of endocrine markers such as chromogranin A. We investigated chromogranin A and secretogranin II immunoreactivity in a series of 208 carcinomas of the large bowel to assess the prevalence and clinical significance of endocrine differentiation. Tumors expressing endocrine markers were classified as low expressors (< than 1 immunoreactive tumour cell/mm2) and high expressors (> than 1 immunoreactive tumour cell/mm2). There were 33 (16%) carcinomas showing both chromogranin A and secretogranin II immunoreactivity: 11 tumours (5%) were high expressors. Endocrine differentiation was not related to the disease stage, tumour location, grade, DNA ploidy and p53 protein accumulation. In the entire series chromogranin A immunoreactivity did not provide prognostic information using univariate and multivariate analysis. A worse overall survival (P = 0.048) was demonstrated for the stage III patients with high expressor tumours, but there were only five patients in this group. The results of our investigation suggest that chromogranin A immunoreactivity is not a useful variable in the prognostic assessment of colorectal adenocarcinomas.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7655739     DOI: 10.1007/bf00192113

Source DB:  PubMed          Journal:  Virchows Arch        ISSN: 0945-6317            Impact factor:   4.064


  36 in total

Review 1.  Integrins: a family of cell surface receptors.

Authors:  R O Hynes
Journal:  Cell       Date:  1987-02-27       Impact factor: 41.582

2.  Clonal origin of columnar, mucous, and endocrine cell lineages in human colorectal epithelium.

Authors:  S C Kirkland
Journal:  Cancer       Date:  1988-04-01       Impact factor: 6.860

3.  Chromogranin: a newly recognized marker for endocrine cells of the human gastrointestinal tract.

Authors:  P Facer; A E Bishop; R V Lloyd; B S Wilson; R J Hennessy; J M Polak
Journal:  Gastroenterology       Date:  1985-12       Impact factor: 22.682

4.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.

Authors:  S M Hsu; L Raine; H Fanger
Journal:  J Histochem Cytochem       Date:  1981-04       Impact factor: 2.479

5.  Neovascularization is associated with a switch to the export of bFGF in the multistep development of fibrosarcoma.

Authors:  J Kandel; E Bossy-Wetzel; F Radvanyi; M Klagsbrun; J Folkman; D Hanahan
Journal:  Cell       Date:  1991-09-20       Impact factor: 41.582

6.  Gastric carcinoid and gastric carcinoma. Morphologic correlates of survival.

Authors:  L W Rogers; R C Murphy
Journal:  Am J Surg Pathol       Date:  1979-06       Impact factor: 6.394

7.  The endodermal origin of the endocrine cells of an adenocarcinoma of the colon of the rat.

Authors:  W F Cox; G B Pierce
Journal:  Cancer       Date:  1982-10-15       Impact factor: 6.860

8.  Immunodetection of secretogranin II in animal and human tissues by new monoclonal antibodies.

Authors:  M Pelagi; A Zanini; A Gasparri; L Ermellino; A M Giudici; S Ferrero; A G Siccardi; R Buffa
Journal:  Regul Pept       Date:  1992-06-11

9.  Cathepsin B expression in colorectal carcinomas correlates with tumor progression and shortened patient survival.

Authors:  E Campo; J Muñoz; R Miquel; A Palacín; A Cardesa; B F Sloane; M R Emmert-Buck
Journal:  Am J Pathol       Date:  1994-08       Impact factor: 4.307

10.  Preparation and characterization of anti-human chromogranin A and chromogranin B (secretogranin I) monoclonal antibodies.

Authors:  M Pelagi; C Bisiani; A Gini; M A Bonardi; P Rosa; P Marè; G Viale; M Grazia Cozzi; M Salvadore; A Zanini
Journal:  Mol Cell Probes       Date:  1989-03       Impact factor: 2.365

View more
  7 in total

1.  Rapid four-month growth of an early-stage adenocarcinoma of the colon with neuroendocrine characteristics.

Authors:  Shigetoshi Hosaka; Kenji Matsuzawa; Kazutoshi Maruyama; Hiroyoshi Ota; Taui Akamatsu; Kendo Kiyosawa
Journal:  Dig Dis Sci       Date:  2003-02       Impact factor: 3.199

Review 2.  Neuroendocrine differentiation: The mysterious fellow of colorectal cancer.

Authors:  Britta Kleist; Micaela Poetsch
Journal:  World J Gastroenterol       Date:  2015-11-07       Impact factor: 5.742

3.  Fetal and neoplastic expression of the neurotensin gene in the human colon.

Authors:  B M Evers; Z Zhou; V Dohlen; S Rajaraman; J C Thompson; C M Townsend
Journal:  Ann Surg       Date:  1996-05       Impact factor: 12.969

Review 4.  The extended granin family: structure, function, and biomedical implications.

Authors:  Alessandro Bartolomucci; Roberta Possenti; Sushil K Mahata; Reiner Fischer-Colbrie; Y Peng Loh; Stephen R J Salton
Journal:  Endocr Rev       Date:  2011-08-23       Impact factor: 19.871

5.  Increased neuroendocrine cells in resected metastases compared to primary colorectal adenocarcinomas.

Authors:  Marco Volante; Valerio Marci; Snezana Andrejevic-Blant; Veronica Tavaglione; Maria Carla Sculli; Marco Tampellini; Mauro Papotti
Journal:  Virchows Arch       Date:  2010-09-02       Impact factor: 4.064

6.  Comparison of neuroendocrine differentiation and KRAS/NRAS/BRAF/PIK3CA/TP53 mutation status in primary and metastatic colorectal cancer.

Authors:  Britta Kleist; Marcel Kempa; Michael Novy; Christian Oberkanins; Li Xu; Guojun Li; Christiane Loland; Micaela Poetsch
Journal:  Int J Clin Exp Pathol       Date:  2014-08-15

Review 7.  Prognostic significance of neuroendocrine differentiation in colorectal adenocarcinoma after radical operation: a meta-analysis.

Authors:  Yu-Jie Zeng; Wei Lai; Lu Liu; Heng Wu; Xing-Xi Luo; Jie Wang; Zhong-Hua Chu
Journal:  J Gastrointest Surg       Date:  2014-02-19       Impact factor: 3.452

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.