Research Update from Dr. Breen regarding aiding prognosis of Canine Diffuse Large B-Cell Lymphoma.
This study involves the evaluation of a cohort of canine lymphoma specimens for the presence of tumor-associated abnormalities associated with four key cancer-associated genes (MYC, BCL6, BCL2 and TP53). The presence of these abnormalities, alone and in combination, has been shown to be predictive of the response to standard treatment modalities in human lymphoma patients, and provides powerful opportunities to predict prognosis in newly diagnosed patients. We hypothesize that the same may apply in dogs.
We have screened the full cohort of canine lymphoma cases for structural and numerical abnormalities involving MYC, BCL6, and BCL2. Overall the data suggest that rearrangement of the genome at the MYC and BCL6 loci is relatively rare within any given case, and occurs at a frequency similar to what is seen in human DLBCL (Li et al. 2018). While BCL2 rearrangement is highly infrequent in dogs (seen in only 2% of cases), and has a generally neutral copy number status, our initial analysis suggests an association of this event with disease-free interval. In an earlier study we showed that the incidence of BCL2 rearrangement and copy number imbalance is low in canine follicular lymphoma (Thomas et al. 2017). The rarity of this B-cell lymphoma subtype in the dog limited the ability to draw generalized comparisons with the human counterpart; however the present study suggests that these observations can be extended to other more common canine B-cell lymphomas. Analysis to date suggests that neither BCL6 nor MYC rearrangement is significantly associated with disease free interval. Assessment of the copy number status of both of these loci concur with previous studies (Thomas et al. 2011), with MYC demonstrating a trend toward copy number gain and BCL6 demonstrating largely neutral copy number status.
DNA sequencing analysis of the TP53 gene has revealed a diverse series of variants among those cases analyzed to date, the majority of which are clustered within a small genomic interval. Almost all variants are simple in structure but are predicted to have a deleterious effect on the function of the gene. We identified variants for which the equivalent alteration is highly recurrent in human tumors, including two key variants that have been reported previously in canine lymphomas, adding to their potential clinical significance. A subset of specimens yielded sequencing data that did not meet our quality control criteria. These specimens showed a high level of DNA degradation, which is likely a consequence of prolonged exposure to formalin during the processing of the biopsy specimen for histologic analysis. Formalin exposure creates crosslinks between DNA and protein, which can confound downstream analyses, including DNA sequencing analysis. We have modified our DNA extraction protocol to ameliorate this factor, and are now reprocessing this subset of cases. Once the new DNA isolations have undergone sequencing analysis we will integrate genomic data for each of the four genes studied, and examine their status in context with patient outcome, to determine their potential as clinically predictive markers for canine lymphoma.