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Article

Elevated Oestrogen Receptor Splice Variant ERαΔ5 Expression in Tumour-adjacent Hormone-responsive Tissue

1
Centre for Biophotonics, Lancaster Environment Centre, Lancaster University, Bailrigg, Lancaster LA1 4YQ, UK
2
Lancashire Teaching Hospitals NHS Trust, Sharoe Green Lane, Fulwood, Preston PR2 9HT, UK
3
Wockhardt Hospitals & Kidney Institute, 111A, Rash Behari Avenue, Kolkata 700029, India
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2010, 7(11), 3871-3889; https://doi.org/10.3390/ijerph7113871
Received: 3 September 2010 / Revised: 27 October 2010 / Accepted: 29 October 2010 / Published: 2 November 2010
(This article belongs to the Special Issue Biomarkers: Environmental Research and Public Health)
Susceptibility to prostate or endometrial cancer is linked with obesity, a state of oestrogen excess. Oestrogen receptor (ER) splice variants may be responsible for the tissue-level of ER activity. Such micro-environmental regulation may modulate cancer initiation and/or progression mechanisms. Real-time reverse transcriptase (RT) polymerase chain reaction (PCR) was used to quantitatively assess the levels of four ER splice variants (ERαΔ3, ERαΔ5, ERβ2 and ERβ5), plus the full-length parent isoforms ERα and ERβ1, in high-risk [tumour-adjacent prostate (n = 10) or endometrial cancer (n = 9)] vs. low-risk [benign prostate (n = 12) or endometrium (n = 9)], as well as a comparison of UK (n = 12) vs. Indian (n = 15) benign prostate. All three tissue groups expressed the ER splice variants at similar levels, apart from ERαΔ5. This splice variant was markedly raised in all of the tumour-adjacent prostate samples compared to benign tissues. Immunofluorescence analysis for ERβ2 in prostate tissue demonstrated that such splice variants are present in comparable, if not greater, amounts as the parent full-length isoform. This small pilot study demonstrates the ubiquitous nature of ER splice variants in these tissue sites and suggests that ERαΔ5 may be involved in progression of prostate adenocarcinoma. View Full-Text
Keywords: endometrial cancer; oestrogen receptor; prostate cancer; real-time RT PCR; splice variant endometrial cancer; oestrogen receptor; prostate cancer; real-time RT PCR; splice variant
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MDPI and ACS Style

Taylor, S.E.; Patel, I.I.; Singh, P.B.; Nicholson, C.M.; Stringfellow, H.F.; Krishna, R.K.G.; Matanhelia, S.S.; Martin-Hirsch, P.L.; Martin, F.L. Elevated Oestrogen Receptor Splice Variant ERαΔ5 Expression in Tumour-adjacent Hormone-responsive Tissue. Int. J. Environ. Res. Public Health 2010, 7, 3871-3889. https://doi.org/10.3390/ijerph7113871

AMA Style

Taylor SE, Patel II, Singh PB, Nicholson CM, Stringfellow HF, Krishna RKG, Matanhelia SS, Martin-Hirsch PL, Martin FL. Elevated Oestrogen Receptor Splice Variant ERαΔ5 Expression in Tumour-adjacent Hormone-responsive Tissue. International Journal of Environmental Research and Public Health. 2010; 7(11):3871-3889. https://doi.org/10.3390/ijerph7113871

Chicago/Turabian Style

Taylor, Siân E., Imran I. Patel, Paras B. Singh, Caroline M. Nicholson, Helen F. Stringfellow, R. K. Gopala Krishna, Shyam S. Matanhelia, Pierre L. Martin-Hirsch, and Francis L. Martin 2010. "Elevated Oestrogen Receptor Splice Variant ERαΔ5 Expression in Tumour-adjacent Hormone-responsive Tissue" International Journal of Environmental Research and Public Health 7, no. 11: 3871-3889. https://doi.org/10.3390/ijerph7113871

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