Title of article
Upregulation of RHOXF2 and ODF4 Expression in Breast Cancer Tissues
Author/Authors
Kazemi-Oula، Golnesa نويسنده Department of Medical Genetics, Tehran University of Medical Sciences, Tehran, Iran , , Ghafouri-Fard، Soudeh نويسنده , , Beigom Mobasheri، Maryam نويسنده Department of Medical Genetics, Tehran University of Medical Sciences, Tehran, Iran , , Geranpayeh، Lobat نويسنده Department of Surgery, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iranran , , Modarressi، Mohammad Hossein نويسنده Department of Medical Genetics, Tehran University of Medical Sciences, Tehran, Iran ,
Issue Information
فصلنامه با شماره پیاپی 67 سال 2015
Pages
27
From page
471
To page
497
Abstract
Objective: During the past decade, the importance of biomarker discovery has been highlighted
in many aspects of cancer research. Biomarkers may have a role in early detection
of cancer, prognosis and survival evaluation as well as drug response. Cancer-testis
antigens (CTAs) have gained attention as cancer biomarkers because of their expression
in a wide variety of tumors and restricted expression in testis. The aim of this study was
to find putative biomarkers for breast cancer.
Materials and Methods: In this applied-descriptive study, the expression of 4 CTAs,
namely acrosin binding protein (ACRBP), outer dense fiber 4 (ODF4), Rhox homeobox
family member 2 (RHOXF2) and spermatogenesis associated 19 (SPATA19) were analyzed
at the transcript level in two breast cancer lines (MCF-7 and MDA-MB-231), 40
invasive ductal carcinoma samples and their adjacent normal tissues as well as 10 fibroadenoma
samples by means of quantitative real-time reverse transcription polymerase
chain reaction (RT-PCR).
Results: All four genes were expressed in both cell lines. Expression of ODF4 and RHOXF2
was detected in 62.5% and 60% of breast cancer tissues but in 22.5 and 17.5% of
normal tissues examined respectively. The expression of both RHOXF2 and ODF4 was
upregulated in cancerous tissues compared with their normal adjacent tissues by 3.31-
and 2.96-fold respectively. The expression of both genes was correlated with HER2/neu
overexpression. RHOXF2 expression but not ODF4 was correlated with higher stages of
tumors. However, no significant association was seen between expression patterns and
estrogen and progesterone receptors status.
Conclusion: ODF4 and RHOXF2 are proposed as putative breast cancer biomarkers
at the transcript level. However, their expression at protein level should be evaluated
in future studies.
Journal title
Cell Journal (Yakhteh)
Serial Year
2015
Journal title
Cell Journal (Yakhteh)
Record number
2277665
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