岡山大学シーズ・ニーズ創出強化イノベーション対話促進プログラム2013　→ Bound for the Future: 【offer information】Okayama University Medical Research Updates （OU-MRU） Vol.81「Innovative method for determining carcinogenicity of chemicals using iPS cells」

Source: Okayama University (JAPAN), Public Relations Division

For immediate release: 07 October 2020

Okayama University research: Innovative method for determining carcinogenicity of chemicals using iPS cells

(Okayama, 07 October) In a recent study published in Scientific Reports researchers at Okayama University use stem cell models to show how certain chemical compounds can induce cancer.

Stem cells have the unique ability to grow into any kind of cell within the body. A subtype of these, cancer stem cells (CSCs), reside within tumors enabling the aggressive growth of cancer. Researchers at Okayama University have previously converted ordinary stem cells into CSCs by growing them in tumor milieu. Now, for the first time, Professor SENO Masaharu and Dr. Juan Du from Okayama University and colleagues used this model and developed a method to observe the induction of cancer stem cells to identify potential carcinogens and their mechanisms.

Stem cells of mice were first grown in the microenvironment of lung tumors. Subsequently, these stem cells were treated with 110 different chemical compounds and the effects of these chemicals on CSC induction was measured. Within just a week, three compounds (PDO325901, CHIR99021, and Dasatinib) led to the first sign of CSCs—spherical cluster formation. While other compounds resulted in the stem cells losing their unique properties, PDO325901, CHIR99021, and Dasatinib effectively upheld the integrity of these cells. The stem cells treated with these three compounds where then transplanted into mice and allowed to grow for 6 weeks. As expected, these cells developed into malignant tumors implicating various parts of the mice. Molecular tags which help recognize CSCs were present in these tumors confirming the successful conversion of stem cells into CSCs.

Cancer is initiated when growth signals within a cell are activated indefinitely. When the team took a deeper look into such signals, they found that one cellular pathway, namely, PI3K-Akt-mTOR was especially active in the newly formed CSCs. Genes involved in this pathway were dormant in the original stem cells, but fully functioning in the CSCs. What’s more, blockers of PI3K-Akt-mTOR did not result in successful CSC formation. PI3K-Akt-mTOR signaling was thus an important factor in turning healthy stem cells cancerous.

“In the current study, we proposed a simple method to assess the risks of tumor-inducing factors in the presence of chemical compounds that accelerated the conversion of miPSCs into CSCs”, conclude the researchers. This study provides a robust model for revealing chemicals with a penchant for cancer initiation, using healthy stem cells. Additionally, this model also unraveled the importance of the PI3K-Akt-mTOR pathway in promoting the conversion of stem cells into CSCs. Therapies which target this pathway might keep cancer cells in check and prevent their spread.

Background

Stem cells and CSCs: Stem cells have two characteristic properties which differentiate them from other cells in the body—they can divide uncontrollably and can grow into any kind of the cell in the body. Given these properties, cancer stem cells (CSCs) are especially dangerous as they multiply easily and contribute to the rapid growth of tumors.

Not too many cellular models enable scientists to visualize the processes at play when healthy, functioning cells turn cancerous; scientists typically rely on existing tumors to study the cells within. Thus, the technique of converting ordinary stem cells into CSCs has opened several research avenues to understand this transition better. Uncovering potential carcinogens, effectiveness of therapies, and underlying pathways are some of the areas researchers can explore with this technique.

Reference

Juan Du, Yanning Xu, Saki Sasada, Aung Ko Ko Oo, Ghmkin Hassan, Hafizah Mahmud, Apriliana Cahya Khayrani, Md Jahangir Alam, Kazuki Kumon, Ryo Uesaki, Said M. Afify, Hager M. Mansour, Neha Nair, Maram H. Zahra, Akimasa Seno, Nobuhiro Okada, Ling Chen, Ting Yan & Masaharu Seno. Signaling Inhibitors Accelerate the Conversion of mouse iPS Cells into Cancer Stem Cells in the Tumor Microenvironment. Scientific Reports, volume.10, Article number: 9955 (2020)

DOI : 10.1038/s41598-020-66471-2
https://www.nature.com/articles/s41598-020-66471-2

Reference (Okayama Univ. e-Bulletin): Professor SENO’s team

Stemming the spread of cancer. (2012)
Cancer stem cell niche: progenies of CSCs maintain properties of CSCs. (2014)
Innovative methods for cancer treatment: World’s first cancer stem cell model from iPS cells. (2015)
Cancer stem cells’ role in tumor growth revealed. (2016)
OU-MRU Vol.34：Novel mouse model for studying pancreatic cancer
OU-MRU Vol.43：Potential origin of cancer-associated cells revealed

Correspondence to
Professor Masaharu Seno, Ph.D.
Department of Biotechnology, Graduate School of
Natural Science and Technology, Okayama University,
3-1-1 Tsushimanaka, Kita-ku, Okayama 700-8530, Japan
e-mail : mseno(a) okayama-u.ac.jp
For inquiries, please contact us by replacing (a) with the @ mark.
http://www.cyber.biotech.okayama-u.ac.jp/senolab/kenkyu-e.html

Further information
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For inquiries, please contact us by replacing (a) with the @ mark.

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