Correction: Androgen receptor is the key transcriptional mediator of the tumor suppressor SPOP in prostate cancer (Cancer Research (2014) 74 (5631-5643) DOI: 10.1158/0008-5472.CAN-14-0476)

Chuandong Geng; Kimal Rajapakshe; Shrijal S. Shah; John Shou; Vijay Kumar Eedunuri; Christopher Foley; Warren Fiskus; Mahitha Rajendran; Sue Anne Chew; Martin Zimmermann; Richard Bond; Bin He; Cristian Coarfa; Nicholas Mitsiades

doi:10.1158/0008-5472.CAN-19-1981

Correction: Androgen receptor is the key transcriptional mediator of the tumor suppressor SPOP in prostate cancer (Cancer Research (2014) 74 (5631-5643) DOI: 10.1158/0008-5472.CAN-14-0476)

Chuandong Geng, Kimal Rajapakshe, Shrijal S. Shah, John Shou, Vijay Kumar Eedunuri, Christopher Foley, Warren Fiskus, Mahitha Rajendran, Sue Anne Chew, Martin Zimmermann, Richard Bond, Bin He, Cristian Coarfa, Nicholas Mitsiades

Research output: Contribution to journal › Comment/debate › peer-review

2 Scopus citations

Abstract

In the original version of this article (1), the duration of exposure to doxycycline (Dox) was incorrectly listed as 24 hours in the legend of Fig. 3A. The figure legend for Fig. 3A has been corrected to indicate the exposure to doxycycline is 72 hours. The error has been corrected in the latest online HTML and PDF versions of the article. The authors regret this error.

Original language	English (US)
Pages (from-to)	4552
Number of pages	1
Journal	Cancer Research
Volume	79
Issue number	17
DOIs	https://doi.org/10.1158/0008-5472.CAN-19-1981
State	Published - Sep 1 2019

ASJC Scopus subject areas

Oncology
Cancer Research

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10.1158/0008-5472.CAN-19-1981

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Geng, C., Rajapakshe, K., Shah, S. S., Shou, J., Eedunuri, V. K., Foley, C., Fiskus, W., Rajendran, M., Chew, S. A., Zimmermann, M., Bond, R., He, B., Coarfa, C., & Mitsiades, N. (2019). Correction: Androgen receptor is the key transcriptional mediator of the tumor suppressor SPOP in prostate cancer (Cancer Research (2014) 74 (5631-5643) DOI: 10.1158/0008-5472.CAN-14-0476). Cancer Research, 79(17), 4552. https://doi.org/10.1158/0008-5472.CAN-19-1981

Correction: Androgen receptor is the key transcriptional mediator of the tumor suppressor SPOP in prostate cancer (Cancer Research (2014) 74 (5631-5643) DOI: 10.1158/0008-5472.CAN-14-0476). / Geng, Chuandong ; Rajapakshe, Kimal; Shah, Shrijal S. et al.
In: Cancer Research, Vol. 79, No. 17, 01.09.2019, p. 4552.

Research output: Contribution to journal › Comment/debate › peer-review

Geng, C , Rajapakshe, K, Shah, SS, Shou, J, Eedunuri, VK, Foley, C, Fiskus, W, Rajendran, M, Chew, SA, Zimmermann, M, Bond, R, He, B, Coarfa, C & Mitsiades, N 2019, 'Correction: Androgen receptor is the key transcriptional mediator of the tumor suppressor SPOP in prostate cancer (Cancer Research (2014) 74 (5631-5643) DOI: 10.1158/0008-5472.CAN-14-0476)', Cancer Research, vol. 79, no. 17, pp. 4552. https://doi.org/10.1158/0008-5472.CAN-19-1981

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abstract = "In the original version of this article (1), the duration of exposure to doxycycline (Dox) was incorrectly listed as 24 hours in the legend of Fig. 3A. The figure legend for Fig. 3A has been corrected to indicate the exposure to doxycycline is 72 hours. The error has been corrected in the latest online HTML and PDF versions of the article. The authors regret this error.",

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AU - Rajapakshe, Kimal

AU - Shah, Shrijal S.

AU - Shou, John

AU - Eedunuri, Vijay Kumar

AU - Foley, Christopher

AU - Fiskus, Warren

AU - Rajendran, Mahitha

AU - Chew, Sue Anne

AU - Zimmermann, Martin

AU - Bond, Richard

AU - He, Bin

AU - Coarfa, Cristian

AU - Mitsiades, Nicholas

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AB - In the original version of this article (1), the duration of exposure to doxycycline (Dox) was incorrectly listed as 24 hours in the legend of Fig. 3A. The figure legend for Fig. 3A has been corrected to indicate the exposure to doxycycline is 72 hours. The error has been corrected in the latest online HTML and PDF versions of the article. The authors regret this error.

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Correction: Androgen receptor is the key transcriptional mediator of the tumor suppressor SPOP in prostate cancer (Cancer Research (2014) 74 (5631-5643) DOI: 10.1158/0008-5472.CAN-14-0476)

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