Induction of blood-circulating bile acids supports recovery from myelosuppressive chemotherapy

Author:

Sigurdsson Valgardur1,Haga Youichi2ORCID,Takei Hajime3ORCID,Mansell Els1,Okamatsu-Haga Chizuko4ORCID,Suzuki Mitsuyoshi1,Radulovic Visnja1,van der Garde Mark15,Koide Shuhei16,Soboleva Svetlana1,Gåfvels Mats7,Nittono Hiroshi3,Ohara Akira2,Miharada Kenichi1ORCID

Affiliation:

1. Division of Molecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden;

2. Department of Pediatrics, Toho University Omori Medical Center, Tokyo, Japan;

3. Junshin Clinic Bile Acid Institute, Tokyo, Japan;

4. Department of Pathology, Tokai University School of Medicine, Kanagawa, Japan;

5. Department of Medicine III, Hematology and Oncology, Technical University of Munich, Munich, Germany;

6. Division of Stem Cell and Molecular Medicine, Center for Stem Cell Biology and Regenerative Medicine, Institute of Medical Science at University of Tokyo, Tokyo, Japan; and

7. Department of Medical Sciences, Uppsala University, Uppsala, Sweden

Abstract

Abstract Chemotherapeutic agents can reduce bone marrow (BM) activity, causing myelosuppression, a common life-threatening complication of cancer treatment. It is challenging to predict the patients in whom prolonged myelosuppression will occur, resulting in a delay or discontinuation of the treatment protocol. An early indicator of recovery from myelosuppression would thus be highly beneficial in clinical settings. In this study, bile acids (BAs) were highly increased in the systemic circulation as a natural response during recovery from myelosuppression, supporting regeneration of BM cells. BA levels in the blood of pediatric cancer patients and mice treated with chemotherapeutic agents were increased, in synchrony with early proliferation of BM cells and recovery from myelosuppression. In a mouse model of altered BA composition, Cyp8b1 knockout mice, a subset of mice recovered poorly after chemotherapy. The poor recovery correlated with low levels and changes in composition of BAs in the liver and systemic circulation. Conversely, BA supplementation in chemotherapy-treated wild-type mice resulted in significantly improved recovery. The results suggest that part of the mechanism by which BAs support recovery is the suppression of endoplasmic reticulum stress pathways in expanding and recovering hematopoietic cells. The findings propose a novel role of BAs as early markers of recovery and active components of the recovery process after chemotherapy.

Publisher

American Society of Hematology

Subject

Hematology

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