%0 Generic %A Kumar Putcha, Balananda-Dhurjati %A Jia, Xu %A Rao Katkoori, Venkat %A Salih, Chura %A Shanmugam, Chandrakumar %A Jadhav, Trafina %A C. Bovell, Liselle %A P. Behring, Michael %A Callens, Tom %A Messiaen, Ludwine %A Bae, Sejong %A Grizzle, William E. %A P. Singh, Karan %A Manne, Upender %D 2015 %T Clinical Implications of Rabphillin-3A-Like Gene Alterations in Breast Cancer %U https://plos.figshare.com/articles/dataset/_Clinical_Implications_of_Rabphillin_3A_Like_Gene_Alterations_in_Breast_Cancer_/1448174 %R 10.1371/journal.pone.0129216 %2 https://plos.figshare.com/ndownloader/files/2109505 %2 https://plos.figshare.com/ndownloader/files/2109506 %2 https://plos.figshare.com/ndownloader/files/2109507 %K ffpe %K breast cancers %K survival %K missense point mutations %K TP 53. RPH 3AL %K snp %K rhp %K RPH 3AL %K tumor suppressor %K rna %K dna %K 17 p 13.1 locus %K loh %K TP 53 loci %K RPH 3AL locus %K utr %K 17 p 13.3 locus %K TP 53 locus %K RPH 3AL gene %X

For the rabphillin-3A-like (RPH3AL) gene, a putative tumor suppressor, the clinical significance of genetic alterations in breast cancers was evaluated. DNA and RNA were extracted from formalin-fixed, paraffin-embedded (FFPE) cancers and matching normal tissues. DNA samples were assessed for loss of heterozygosity (LOH) at the 17p13.3 locus of RPH3AL and the 17p13.1 locus of the tumor suppressor, TP53. RPH3AL was sequenced, and single nucleotide polymorphisms (SNPs) were genotyped. RNA samples were evaluated for expression of RPH3AL, and FFPE tissues were profiled for its phenotypic expression. Alterations in RPH3AL were correlated with clinicopathological features, LOH of TP53, and patient survival. Of 121 cancers, 80 had LOH at one of the RPH3AL locus. LOH of RHP3AL was associated with nodal metastasis, advanced stage, large tumor size, and poor survival. Although ~50% were positive for LOH at the RPH3AL and TP53 loci, 19 of 105 exhibited LOH only at the RPH3AL locus. Of these, 12 were non-Hispanic Caucasians (Whites), 15 had large tumors, and 12 were older (>50 years). Patients exhibiting LOH at both loci had shorter survival than those without LOH at these loci (log-rank, P = 0.014). LOH at the TP53 locus alone was not associated with survival. Analyses of RPH3AL identified missense point mutations in 19 of 125 cases, a SNP (C>A) in the 5’untranslated region at -25 (5’UTR-25) in 26 of 104, and a SNP (G>T) in the intronic region at 43 bp downstream to exon-6 (intron-6-43) in 79 of 118. Genotype C/A or A/A of the SNP at 5’UTR-25 and genotype T/T of a SNP at intron-6-43 were predominantly in Whites. Low levels of RNA and protein expression of RPH3AL were present in cancers relative to normal tissues. Thus, genetic alterations in RPH3AL are associated with aggressive behavior of breast cancers and with short survival of patients.

%I PLOS ONE