Aberrant expression of the PHF14 gene in biliary tract cancer cells

DNA copy number aberrations in human biliary tract cancer (BTC) cell lines were investigated using a high-density oligonucleotide microarray. A novel homozygous deletion was detected at chromosomal region 7p21.3 in the OZ cell line. Further validation experiments using genomic PCR revealed a homozyg...

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Veröffentlicht in:Oncology letters 2013-06, Vol.5 (6), p.1849-1853
Hauptverfasser: AKAZAWA, TAKAKO, YASUI, KOHICHIROH, GEN, YASUYUKI, YAMADA, NOBUHISA, TOMIE, AKIRA, DOHI, OSAMU, MITSUYOSHI, HIRONORI, YAGI, NOBUAKI, ITOH, YOSHITO, NAITO, YUJI, YOSHIKAWA, TOSHIKAZU
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Sprache:eng
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Zusammenfassung:DNA copy number aberrations in human biliary tract cancer (BTC) cell lines were investigated using a high-density oligonucleotide microarray. A novel homozygous deletion was detected at chromosomal region 7p21.3 in the OZ cell line. Further validation experiments using genomic PCR revealed a homozygous deletion of a single gene, plant homeodomain (PHD) finger protein 14 (PHF14). No PHF14 mRNA or protein expression was detected, thus demonstrating the absence of PHF14 expression in the OZ cell line. Although the PHD finger protein is considered to be involved in chromatin-mediated transcriptional regulation, little is known about the function of PHF14 in cancer. The present study observed that the knock down of PHF14 using small interfering RNA (siRNA) enhanced the growth of the BTC cells. These observations suggest that aberrant PHF14 expression may have a role in the tumorigenesis of BTC.
ISSN:1792-1074
1792-1082
DOI:10.3892/ol.2013.1278