9 research outputs found
Novel Alleles of the D16S752 Polymorphic Genetic Marker Linked to E-Cadherin Gene ā A Potential Population Marker
Seven DNA variants that polymorphic genetic marker D16S752 reveals in Croatian
population are reported in this paper. The marker is a GATA tetranucleotide repeat
linked to human E-cadherin gene (CDH1). Prior studies involving this marker revealed
only four DNA allele variants. The reported DNA variants contribute to the collection of
hypervariable DNA polymorphisms data useful in the field of anthropological and population
genetic and forensic medicine
nm23-H1 expression and loss of heterozygosity in colon adenocarcinoma
Background: The discovery that genetic alterations in oncogenes and tumour suppressor genes accompany tumour formation in many human tumours has encouraged the search for genes that promote or suppress tumour spread and metastasis; nm23 is a promising candidate for a metastasis suppressing gene. Aims: To evaluate whether expression of nm23-H1 protein or loss of heterozygosity (LOH) of the nm23-H1 gene is associated with colon cancer progression. Materials/Methods: Paraffin wax embedded tissue sections were analysed immunohistochemically. DNA isolated from normal and tumour tissue was used for LOH analysis using a variable nucleotide tandem repeat (VNTR) marker located in the untranslated 5ā² region of the nm23-H1 gene. RNA isolated from tumour and normal tissue was used for āreal timeā RT-PCR. Results: Of 102 adenocarcinomas examined, 58.8% stained weakly for nm23-H1 protein. There was a negative correlation between nm23-H1 positivity and tumour histological grade. In VNTR analysis, 70.2% of patients were informative and 27.4% of tumours had nm23-H1 LOH. There was a positive correlation between nm23-H1 LOH and both tumour histological grade and Dukesās stage. Expression of nm23-H1 mRNA was increased in 22 of 30 colon tumours compared with normal tissue. No significant correlation was found between nm23-H1 mRNA expression and histological grade or Dukesās stage of tumours. Conclusions: These findings suggest that nm23-H1 protein expression in early stages may have a role in suppressing metastasis in sporadic colon cancer, whereas at a later stage both reduced nm23-H1 protein expression and LOH of the nm23-H1 gene may play role in colon cancer progression and metastasis