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Researchers discover novel mechanism to stop the spread of breast cancer

Date:
November 23, 2016
Source:
National University of Singapore
Summary:
Controlling the levels of the TIP60 protein, which is a tumor suppressor, could potentially prevent the spread of breast cancer cells, a team of has found.
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A team of researchers from the Cancer Science Institute of Singapore (CSI Singapore) at the National University of Singapore (NUS) has found that controlling the levels of the TIP60 protein, which is a tumor suppressor, could potentially prevent the spread of breast cancer cells.

Specifically, the research team that is led by Assistant Professor Sudhakar Jha from CSI Singapore discovered that TIP60 interacts with two other proteins called DNMT1 and SNAIL2, to inhibit the spread of cancer cells. This is the first study which reports the novel function of TIP60 in regulating DMNT1-SNAIL2 axis, and subsequently inhibiting metastasis, which is the spread of cancer cells to other parts of the body.

"In this study, we found that the absence of TIP60 raises the levels of DNMT1, resulting in the activation of SNAIL-2 function. When this molecular program is turned on, epithelial cells -- which protect or enclose organs -- acquire migratory and invasive properties. This leads to the spreading of cancer cells. Understanding this mechanism holds the important key to suppressing the migration of cancer cells," explained Mr Zhang Yanzhou, a final year PhD student from CSI Singapore's Graduate Programme in Cancer Biology, and first author of the study.

This is an important discovery for breast cancer patients with poor Overall Survival (OS) and Disease-Free Survival (DFS) prognoses, as it was previously found that TIP60 levels in these patients are low, thus reducing their defence against cancer cell metastasis.

The team's discovery may have important implications for other cancers as patients with colon and cervical cancers have also been found to have irregular TIP60 levels. Hence, the direction of this study may open doors to potential treatment of different types of cancers in the future.

"This study provides important evidence that TIP60 levels could possibly serve as prognostic marker of breast cancer progression, and the stabilisation of TIP60 could be a promising strategy to treat cancers. We are currently developing inhibitors which can increase TIP60 levels and in turn, prevent the spread of cancer. Moving forward, we are also looking into collaborating with clinician scientists from the National University Health System to initiate clinical trials using DNMT1 inhibitors to treat breast cancer patients and decrease metastasis by targeting cells that have lower levels of TIP60 as these cells are more likely to be invasive," said Asst Prof Jha.

The findings of the study were published in the Journal of Molecular Cell Biology in September 2016.


Story Source:

Materials provided by National University of Singapore. Note: Content may be edited for style and length.


Journal Reference:

  1. Yanzhou Zhang, Vanitha Krishna Subbaiah, Deepa Rajagopalan, Cheng Yong Tham, Lissa Nurrul Abdullah, Tan Boon Toh, Min Gong, Tuan Zea Tan, Shweta Pradip Jadhav, Amit Kumar Pandey, Neerja Karnani, Edward Kai-Hua Chow, Jean Paul Thiery, Sudhakar Jha. TIP60 inhibits metastasis by ablating DNMT1−SNAIL2-driven epithelial-mesenchymal transition program. Journal of Molecular Cell Biology, 2016; 8 (5): 1 DOI: 10.1093/jmcb/mjw038

Cite This Page:

National University of Singapore. "Researchers discover novel mechanism to stop the spread of breast cancer." ScienceDaily. ScienceDaily, 23 November 2016. <www.sciencedaily.com/releases/2016/11/161123090659.htm>.
National University of Singapore. (2016, November 23). Researchers discover novel mechanism to stop the spread of breast cancer. ScienceDaily. Retrieved December 21, 2024 from www.sciencedaily.com/releases/2016/11/161123090659.htm
National University of Singapore. "Researchers discover novel mechanism to stop the spread of breast cancer." ScienceDaily. www.sciencedaily.com/releases/2016/11/161123090659.htm (accessed December 21, 2024).

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