Investigating a Genetic Basis of Urogenital Cancer in California Sea Lions (Zalophus californianus)
IAAAM 2013
Helen M. Browning1*+; Ailsa J. Hall1; Kathleen M. Colgrove2; Frances M.D. Gulland3; Mark P. Dagleish4; John A. Hammond5
1Centre for Marine Animal Health and Sea Mammal Research Unit, University of St Andrews, St Andrews, Fife, KY16 8LB, UK; 2Veterinary Diagnostic Laboratory, College of Veterinary Medicine, University of Illinois, Urbana, Illinois, 61802; 3Veterinary Science Department, Center for Marine Animal Health and The Marine Mammal Center, California, 94965 USA; 4Moredun Research Institute, Penicuik, Midlothian, EH26 0PZ, UK; 5The Pirbright Institute, Pirbright, Surrey, GU24 0NF

Abstract

The California sea lion (Z. californianus) has an unusually high occurrence of urogenital carcinoma, with one study revealing metastatic carcinoma in 18% of animals admitted to a rehabilitation centre over a 15 year period.2 It is likely that the aetiology of this disease is multi-factorial as genetics, viral infection and exposure to contaminants have been associated with this cancer to date. This study concentrates on one area; the potential involvement of genetic factors. A previous investigation into a genetic link found cancer to be more likely in animals with specific microsatellite marker alleles1 with the marker Pv11 appearing to be significantly associated with the development of the disease1. This marker is found within an intron of a gene called HPSE2 which codes for the protein heparanase 2. HPSE2 shares approximately 40% sequence homology with the HPSE1 gene which is associated with cancer metastasis.4 Therefore a gene which demonstrates homology to it is of potential clinical interest. Recent work into cervical neoplasia in humans has identified an increase in expression of HPSE2 with increasing severity of neoplastic lesion.3 The objective of this study is to characterise the HPSE2 gene in Z. californianus using cervical tissue from animals of known Pv11 genotype. To do this RNA was extracted from six cervical tissue samples and converted to cDNA. PCR reactions were then carried out to target splice variants of HPSE2 expression followed by cloning of products. Sequencing of positive clones resulted in a high identity to the domestic dog (Canis lupus familiaris) heparanase 2 transcript variant 2 via Basic Local Alignment Search Tool (BLAST) confirming the presence of at least one HPSE2 isoform in Z. californianus. In order to investigate differences in expression of HPSE2 in animals suffering from neoplasia and control animals 15 cervical tissue samples were examined. These consisted of nine samples from cancer positive animals and six from control animals. Immunohistochemical assays were carried out on the samples using polyclonal HPSE2 antibody. All of the samples from the control animals stained negative and only three out of the nine cancer animals stained positive. However, all three positive samples were from animals of the same Pv11 genotype. This could suggest that Pv11 genotype is important with regards to HPSE2 expression in cervical cancer but further studies are necessary to confirm this.

* Presenting author
+ Student presenter

Acknowledgements

The authors would like to thank Dr Denise Greig, Lauren Rust - The Marine Mammal Center and Tanya Sneddon - University of St Andrews, Jeanie Finlayson - Moredun Research Institute and Karen Billington - Institute of Animal Health, Berkshire, UK for technical assistance.

Literature Cited

1.  Acevedo-Whitehouse K, Gulland F, Greig D, Amos W. 2003. Disease susceptibility in California Sea Lions. Nature. 422: 35.

2.  Gulland FMD, Trupkiewicz JG, Spraker TR, Lowenstine LJ. 1996. Metastatic carcinoma of probable transitional cell origin in 66 free-living California sea lions (Zalophus californianus), 1979 to 1994. J Wildl Dis. 32(2):250–258.

3.  Marques RM, Focchi GR, Castelo A, Pinhal MA, Nicolau SM. 2012. The immunoexpression of heparanase 2 in normal epithelium, intraepithelial, and invasive squamous neoplasia of the cervix. J Low Genit Tract Dis. 16(3):256–262.

4.  McKenzie E, Tyson K, Stamps A, Smith P, Turner P, Barry R, Hircock M, Patel S, Barry E, Stubberfield C, Terrett J, Page M. 2000. Cloning and Expression Profiling of Hpa2, a Novel Mammalian Heparanase Family Member. Biochem Biophys Res Commun. 276:1170–1177.

  

Speaker Information
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Helen M. Browning
Centre for Marine Animal Health and Sea Mammal Research Unit
University of St Andrews
St Andrews, Fife, UK


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