MAIN


©1996-2018. All Rights Reserved. Online Journal of Veterinary Research. You may not store these pages in any form except for your own personal use. All other usage or distribution is illegal under international copyright treaties. Permission to use any of these pages in any other way besides the before mentioned must be gained in writing from the publisher. This article is exclusively copyrighted in its entirety to OJVR. This article may be copied once but may not be, reproduced or re-transmitted without the express permission of the editors. This journal satisfies the refereeing requirements (DEST) for the Higher Education Research Data Collection (Australia). Linking:To link to this page or any pages linking to this page you must link directly to this page only here rather than put up your own page.


OJVRTM

Online Journal of Veterinary Research©

 

Volume 18(7): 528-542,  2014. Redacted 2017.


Histopathological studies on canine mammary tumors with special reference to p53 gene mutations

 

Hemanth I, Kumar R, Varshney KC*, Nair MG, Thanislass J1, Sivakumar M2, Ramesh Kumar B3

 

Dept(s) of Veterinary Pathology, 1Biochemistry, 2Anatomy & Histology 3Surgery & Radiology Rajiv Gandhi Institute of Veterinary Education and Research, Puducherry, Pondicherry, India. *Corresponding Author:

 

ABSTRACT

 

Hemanth I, Kumar R, Varshney KC, Nair MG, Thanislass J, Sivakumar M, Ramesh Kumar B., Histopathological studies on canine mammary tumors with special reference to p53 gene mutations. Onl J Vet Res., 18(7): 528-542,  2014. Canine mammary neoplasms are the most common neoplastic condition accounting for ~52% of all tumors in bitches. One-third to a half are malignant. Because tumor suppressor genes are involved in the origin and progression of human and canine neoplasms, mutational status can be used for prognosis. Histopathological grading, histochemical characteristics and incidence of p53 gene mutations from 10 canine mammary tumors is reported. Two tumors were benign and 8 malignant. Histological grading of the carcinomas showed 12.50% well differentiated grade I, 50% moderately differentiated grade II and 37.25% grade III (poorly differentiated), neoplasm PCR-SSCP analysis of DNA isolated from 10 samples for exons 5-8 of p53 gene revealed 7 mutations in 3 samples of which 3 ductal carcinomas had mutations in 4 codons 147, 148, 149 and 150 and two each had mis-sense and silent types within exon 5. Tubulo-papillary adenocarcinomas showed mutations in 2 codons 126 and 158, one each of mis-sense and silent types within exon 5. Benign mixed mammary tumor revealed single silent mutation involving the codon 188 of exon 6. Presence of p53 gene mutations in canine mammary tumor samples in our study correlated with histological aggressiveness (higher histological grades) of respective neoplasms.

 

Key words: Canine mammary tumors – histopathology – mutations - p53 tumor suppressor gene – Polymerase chain reaction – Single strand

conformation polymorphism.


MAIN

FULL-TEXT (SUBSCRIPTION OR PURCHASE TITLE $25USD)