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DEAD-box helicase DP103 defines metastatic potential of human breast cancers
Eun Myoung Shin, … , Alan Prem Kumar, Vinay Tergaonkar
Eun Myoung Shin, … , Alan Prem Kumar, Vinay Tergaonkar
Published August 1, 2014
Citation Information: J Clin Invest. 2014;124(9):3807-3824. https://doi.org/10.1172/JCI73451.
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Research Article Oncology Article has an altmetric score of 36

DEAD-box helicase DP103 defines metastatic potential of human breast cancers

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Abstract

Despite advancement in breast cancer treatment, 30% of patients with early breast cancers experience relapse with distant metastasis. It is a challenge to identify patients at risk for relapse; therefore, the identification of markers and therapeutic targets for metastatic breast cancers is imperative. Here, we identified DP103 as a biomarker and metastasis-driving oncogene in human breast cancers and determined that DP103 elevates matrix metallopeptidase 9 (MMP9) levels, which are associated with metastasis and invasion through activation of NF-κB. In turn, NF-κB signaling positively activated DP103 expression. Furthermore, DP103 enhanced TGF-β–activated kinase-1 (TAK1) phosphorylation of NF-κB–activating IκB kinase 2 (IKK2), leading to increased NF-κB activity. Reduction of DP103 expression in invasive breast cancer cells reduced phosphorylation of IKK2, abrogated NF-κB–mediated MMP9 expression, and impeded metastasis in a murine xenograft model. In breast cancer patient tissues, elevated levels of DP103 correlated with enhanced MMP9, reduced overall survival, and reduced survival after relapse. Together, these data indicate that a positive DP103/NF-κB feedback loop promotes constitutive NF-κB activation in invasive breast cancers and activation of this pathway is linked to cancer progression and the acquisition of chemotherapy resistance. Furthermore, our results suggest that DP103 has potential as a therapeutic target for breast cancer treatment.

Authors

Eun Myoung Shin, Hui Sin Hay, Moon Hee Lee, Jen Nee Goh, Tuan Zea Tan, Yin Ping Sen, See Wee Lim, Einas M. Yousef, Hooi Tin Ong, Aye Aye Thike, Xiangjun Kong, Zhengsheng Wu, Earnest Mendoz, Wei Sun, Manuel Salto-Tellez, Chwee Teck Lim, Peter E. Lobie, Yoon Pin Lim, Celestial T. Yap, Qi Zeng, Gautam Sethi, Martin B. Lee, Patrick Tan, Boon Cher Goh, Lance D. Miller, Jean Paul Thiery, Tao Zhu, Louis Gaboury, Puay Hoon Tan, Kam Man Hui, George Wai-Cheong Yip, Shigeki Miyamoto, Alan Prem Kumar, Vinay Tergaonkar

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Figure 2

DP103 regulates invasive abilities of cancer cells.

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DP103 regulates invasive abilities of cancer cells.
(A) MDA-MB-231 cells...
(A) MDA-MB-231 cells transfected with control siRNA (ctsi) and 2 different siRNAs against DP103. Scratch wound healing assay is shown. (B) MDA-MB-231 cells represented in percentage of siDP103 or ctsi cell movement after scratching. *P < 0.05. (C) MDA-MB-231 and BT549 cells transfected with control siRNA (ctsi) and 2 different siRNAs against DP103 in Transwell assays. Inset shows representative photograph. (D) Quantification of MDA-MB-231 cells invaded through Transwell invasion chambers from C. *P < 0.05. (E) Quantification of BT549 cells invaded through the Transwell invasion chambers from C. *P < 0.05. (F) MCF10A cells transfected with control pcDNA3 vector (EV) and pcDNA3-FLAG-DP103 (DP103). Cell extracts immunoblotted with anti-DP103 and anti–β-actin antibodies. (G) MCF10A cells transfected as in F and analyzed in an invasion assay as in C. (H) MCF10A cells that invaded through the chambers quantified and represented. *P < 0.05. (I) Pulmonary and liver metastases from primary tumors evaluated by bioluminescence imaging. Color scale depicts photon flux (p/s) emitted from the organs. (J) Left: DP103 expression in primary tumor injected with empty vector–transfected MDA-MB-231 cells (MDA-MB-231-EV). Right: DP103 expression in mouse mammary fat pad injected with DP103-transfected cells (MDA-MB-231-DP103). (K) Distal metastasis to lung tissues quantified by mRNA levels of human GAPDH. *P = 0.05. (L) Metastasis to liver tissues quantified by mRNA levels of human GAPDH. *P = 0.05. Fold difference in protein expression indicated in F. Original magnification, ×10; ×40 (insets).

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ISSN: 0021-9738 (print), 1558-8238 (online)

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