Literature DB >> 17465446

Histopathological and genetic differences between polypoid and non-polypoid submucosal colorectal carcinoma.

Ichiro Hirata1, Fang-Yu Wang, Mitsuyuki Murano, Takuya Inoue, Ken Toshina, Takashi Nishikawa, Kentaro Maemura.   

Abstract

AIM: To investigate the histopathological and genetic differences between polypoid growth (PG) and non-polypoid growth (NPG) submucosal invasive colorectal carcinoma (CRC).
METHODS: A total of 96 cases of submucosal CRC were divided into two groups according to their growth type; 60 cases of PG and 36 cases of NPG. The size, histological degree of dysplasia, depth of submucosal invasion and lymph node metastasis were compared between the two groups. Furthermore, expression of p53 was detected by immunohistochemical staining, and K-ras gene mutation was examined by polymerase chain reaction based single-strand conformation polymorphism (SSCP).
RESULTS: The average size of the lesions in the NPG group was significantly smaller than those in the PG group (7.5 mm vs 13.8 mm, P<0.001). The histological degree of dysplasia tended to be more severe in NPG group, while the incidence of submucosal massive invasion and the lymph node metastasis were both significantly higher in the NPG type than in the PG group (64.3% vs 43.3%, P=0.004; 43% vs 7%, P=0.008, respectively). In addition, K-ras gene mutations were detected in 67% of lesions in the PG group, but none in the NPG group, while no difference in p53 immunohistochemical expression was found between the two groups.
CONCLUSION: Compared with PG submucosal CRC, NPG type demonstrates more frequent submucosal massive invasion, more lymph node metastasis and a higher degree dysplasia. Genetically, NPG type shows much less frequent K-ras mutation.

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Year:  2007        PMID: 17465446      PMCID: PMC4319123          DOI: 10.3748/wjg.v13.i14.2048

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  31 in total

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2.  Associations of Ki-ras proto-oncogene mutation and p53 gene overexpression in sporadic colorectal adenomas with demographic and clinicopathologic characteristics.

Authors:  Janine G Einspahr; Maria Elena Martinez; Ruiyun Jiang; Chiu-Hsieh Hsu; Asif Rashid; Achyut K Bhattacharrya; Dennis J Ahnen; Elizabeth T Jacobs; P Scott Houlihan; C Renee Webb; David S Alberts; Stanley R Hamilton
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2006-08       Impact factor: 4.254

3.  Frequent involvement of ras-signalling pathways in both polypoid-type and flat-type early-stage colorectal cancers.

Authors:  H Noda; Y Kato; H Yoshikawa; M Arai; K Togashi; H Nagai; F Konishi; Y Miki
Journal:  J Exp Clin Cancer Res       Date:  2006-06

4.  Diagnostic criteria for gastrointestinal carcinomas in Japan and Western countries: proposal for a new classification system of gastrointestinal epithelial neoplasia.

Authors:  R J Schlemper; Y Kato; M Stolte
Journal:  J Gastroenterol Hepatol       Date:  2000-10       Impact factor: 4.029

5.  Depressed-type (0-IIc) colorectal neoplasm in patients with family history of first-degree relatives with colorectal cancer: A cross-sectional study.

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Journal:  World J Gastroenterol       Date:  2006-05-21       Impact factor: 5.742

6.  Distinct chromosomal imbalances in nonpolypoid and polypoid colorectal adenomas indicate different genetic pathways in the development of colorectal neoplasms.

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Review 7.  Genetic models of human cancer as a multistep process. Paradigm models of colorectal cancer, breast cancer, and chronic myelogenous and acute lymphoblastic leukaemia.

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Review 8.  Pathogenesis of colorectal cancer.

Authors:  Jeremy R Jass
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9.  Advanced colorectal polyps with the molecular and morphological features of serrated polyps and adenomas: concept of a 'fusion' pathway to colorectal cancer.

Authors:  J R Jass; K Baker; I Zlobec; T Higuchi; M Barker; D Buchanan; J Young
Journal:  Histopathology       Date:  2006-08       Impact factor: 5.087

10.  Does early polypoid colorectal cancer with depression have a pathway other than adenoma-carcinoma sequence?

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Journal:  Tumori       Date:  2003 Jul-Aug
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