Author/Authors :
Norhaifa، G. نويسنده Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia , , Bachek، N. F. نويسنده Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia , , Kamarudin، N. H. نويسنده Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia , , Nashreq، K. N. نويسنده Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia , , Ajat، M. M. نويسنده Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia , , Hafandi، A. نويسنده Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia , , Selvarajah، G. T. نويسنده Department of Veterinary Clinical Studies, Faculty of Veterinary Medicine, Universiti Putra Malaysia , , Hezmee، M. N. M. نويسنده Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia ,
Abstract :
A study of the development of spontaneous tumours in dogs gives many benefits in oncology research
due to the similarity between dog and human cancer in terms of epidemiologic, biologic and clinical
features. There is evidence that the complement component 5 anaphylatoxin (C5a) and its receptor are
involved in the development of many types of tumour due to its inflammatory properties. The purpose
of this study was to determine the expression of C5a on several types of canine spontaneous tumour
i.e. mammary tumour, lung tumour, testicular tumour and melanoma. The expression of C5a in these
tumours was compared with normal tissue from the breasts, lungs, testes and skin. The total of eight
post-mortem canine tissues were collected from University Veterinary Hospital (UVH), University
Putra Malaysia and stored in a preservative solution (RNAlater) to keep the RNA from degrading. The
RNA was extracted using the Qiagen RNA Extraction Kit and a cDNA synthesis was carried out using
a one-step PCR kit (Promega, USA). The expression of C5a was determined using reverse transcriptase
PCR (RT-PCR) and Quantitative real-time PCR (qPCR) techniques. The results showed that all types
of tumour gave higher expression of C5a compared to normal tissue. This means that the CT value for
the tumours was below 30 cycles except for melanoma and the expression of C5a of normal tissues was
above 30 cycles. This finding suggests that C5a and its receptor may be involved in the development
of tumours in dogs and can be used as a tumour biomarker for both animals and humans in the future.Nevertheless, further studies investigating the
mechanisms of C5a and its receptor in canine
spontaneous tumour are necessary.