Repurposing cancer drugs: An innovative therapeutic strategy to fight bone cancer.

August.03.2021RESEARCH HIGHLIGHTS

Source: Okayama University (JAPAN), Public Relations Division
For immediate release: 3 August 2021
Okayama University research: Repurposing cancer drugs: An innovative therapeutic strategy to fight bone cancer.

(Okayama, 3 August) In a study reported in the journal Molecular Cancer Therapeutics, researchers from Okayama University describe the effects of pexidartinib, a drug targeting macrophages infiltrating into a tumor, for bone and soft-tissue malignancies.

Sarcoma is a rare form of cancer that often originates within bones and then spreads to other organs. A distinct feature of cancer and sarcoma is the presence of tumor-associated macrophages (TAMs). These are usually healthy blood cells which have been converted by cancer cells to turn against the body and help their perpetrators spread. Now, in a collaboration between Okayama University and the Memorial Sloan Kettering Cancer Center, a research team has shown that PLX3397 (pexidartinib), a drug that can inhibit the formation of TAMs, is effective in mitigating the spread of sarcoma.

Colony stimulating factor 1 (CSF-1) is a cytokine secreted by cancer cells which oversees the creation of TAMs. PLX3397 is known to effectively inhibit CSF-1/CSF-1 receptor (CSF-1R) on TAMs. Now, in this study the researchers investigated whether this ability of PLX3397 could be leveraged in sarcoma too.

Sarcoma cells were first analyzed to confirm that they secreted CSF-1. Next, blood cells were extracted from mice and grown in the same environment as these sarcoma cells. Subsequently, the blood cells started proliferating faster and showing TAM-like tendencies. When the genetic makeup of these nascent TAMs was assessed, the team found showed that they had transformed into M2-like macrophages, a subtype that indeed promotes tumor growth. The mixture of cells was then treated with varying doses of PLX3397 to find that the drug curbed the transformation, growth, and movement of TAMs.

Next, the effects of PLX3397 in a mouse model of bone cancer were examined. Sarcoma cells were transplanted into the tibial bones of mice and monitored for a few weeks. By the end of 3 weeks, the cancer had grown and spread into the lungs of these mice. However, mice who had been treated with high doses of PLX3397 not only showed smaller tumors within their bones, but also displayed no signs of cancer within their lungs. Lastly, the team extracted tumor tissues from these mice to study the cancer cells closely. It was found that PLX3397 also increased the presence of cancer-fighting immune cells, CD8 T cells, within these tumors. PLX3397 thus showed an effective inhibition of sarcoma in cellular and animal models.

“Our preclinical results show that PLX3397 has strong macrophage- and T cell-modulating effects that may translate into cancer immunotherapy for bone and soft tissue sarcomas,” conclude the researchers. Although successful results still need to be shown in human clinical trials, this study paves the way for an effective new way to tackle sarcoma.

Background
Sarcoma: Sarcoma is a form of cancer that originates within bone tissue or soft tissues such as the muscles, fat, or tendons. The former type, osteosarcoma, is the most common subtype of bone cancer and affects mostly teens and young adults. Sarcomas have a high potential of spread to distant organs, predominantly to the lungs.

At present, nearly a third of patients respond very poorly to the available therapies for sarcoma. Thus, development of targeted therapies and/or immunotherapies for bone and soft-tissue sarcomas is crucial.

Tumor-associated macrophages (TAMs): In certain forms of cancer, innocuous blood cells are recruited by cancerous ones and converted into specialized immune cells called TAMs. Under usual circumstances, macrophages help the body ward off invaders and combat infection (M1-like macrophages). However, the CSF-1 secreted by cancer cells within the tumor milieu generates macrophages which promote the growth and progression of tumors (M2-like macrophages). Owing to this property, inhibition of CSF-1/CSF-1R is being investigated as a therapeutic target against TAMs in the different cancerous tissues.

Reference
Tomohiro Fujiwara, Mohamed A. Yakoub, Andrew Chandler, Alexander B. Christ, Guangli Yang, Ouathek Ouerfelli, Vinagolu K. Rajasekhar, Aki Yoshida, Hiroya Kondo, Toshiaki Hata, Hiroshi Tazawa, Yildirim Dogan, Malcom A.S. Moore, Toshiyoshi Fujiwara, Toshifumi Ozaki, Ed Purdue, John H. Healey. CSF-1/CSF-1R Signaling Inhibitor Pexidartinib (PLX3397) Reprograms Tumor-Associated Macrophages and Stimulates T-Cell Infiltration in the Sarcoma Microenvironment. Molecular Cancer Therapeutics, 2021 Jun 4;molcanther.0591.2020.
DOI: 10.1158/1535-7163.MCT-20-0591
CSF1/CSF1R Signaling Inhibitor Pexidartinib (PLX3397) Reprograms Tumor-Associated Macrophages and Stimulates T-cell Infiltration in the Sarcoma Microenvironment | Molecular Cancer Therapeutics

Correspondence to
Assistant Professor FUJIWARA Tomohiro, M.D.,Ph.D.
Department of Orthopaedic Surgery,
Graduate School of Medicine, Dentistry and Pharmaceutical Science,
Okayama University, 2-5-1 Shikata-cho, Kita-ku,
Okayama 700-8558, Japan
E-mail: tomomedvn(a)okayama-u.ac.jp
For inquiries, please contact us by replacing (a) with the @ mark.

Further information
Okayama University
1-1-1 Tsushima-naka , Kita-ku , Okayama 700-8530, Japan
Public Relations Division
E-mail: www-adm(a) adm.okayama-u.ac.jp
For inquiries, please contact us by replacing (a) with the @ mark.
Website: //www.okayama-u.ac.jp/index_e.html
Okayama Univ. e-Bulletin: //www.okayama-u.ac.jp/user/kouhou/ebulletin/
We love OKAYAMA UNIVERSITY: https://www.youtube.com/watch?v=7cXlttQIk3E
Okayama University Image Movie(2020)
https://www.youtube.com/watch?v=BKRoF0tffmA
Okayama University supports the Sustainable Development Goals: https://sdgs.okayama-u.ac.jp/en/


A. The growth of TAMs was curbed with increasing doses of PLX3397 treatment.
B. The growth of tumors at the site of transplantation (circled) was greatly contained with high doses of PLX3397 compared to the control (PBS).

ACADEMIC YEAR