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Efficacy of Recombinant Methioninase on Late-stage Patient Cancer in the Histoculture Drug Response Assay (HDRA) as a Potential Functional Biomarker of Sensitivity to Methionine-restriction Therapy in the Clinic.
Kubota, Yutaro; Sasaki, Masato; Han, Qinghong; Hozumi, Chihiro; Tsunoda, Takuya; Hoffman, Robert M.
Afiliación
  • Kubota Y; AntiCancer Inc., San Diego, CA, U.S.A.
  • Sasaki M; Department of Surgery, University of California, San Diego, CA, U.S.A.
  • Han Q; Division of Internal Medicine, Department of Medical Oncology, Showa University School of Medicine, Tokyo, Japan.
  • Hozumi C; University of Fukui Faculty of Medical Sciences, Department of Thoracic Surgery, Fukui, Japan.
  • Tsunoda T; AntiCancer Inc., San Diego, CA, U.S.A.
  • Hoffman RM; AntiCancer Japan Inc., Narita, Japan.
Cancer Diagn Progn ; 4(3): 239-243, 2024.
Article en En | MEDLINE | ID: mdl-38707720
ABSTRACT
Background/

Aim:

The present study utilized the three-dimensional histoculture drug response assay (HDRA) to determine the efficacy of recombinant methioninase (rMETase) on tumor tissue resected from patients with late-stage cancer, as a functional biomarker of sensitivity to methionine restriction therapy. Patients and

Methods:

Resected peritoneal-metastatic cancer, including colorectal cancer, pancreatic cancer, ovarian cancer, and pseudomyxoma were placed on Gelform in RPMI 1640 medium for seven days and treated with rMETase from 2.5 U/ml to 20 U/ml. Cell viability was determined using the MTT assay. A total of 48 patients with late-stage cancer underwent testing for rMETase responsiveness using the HDRA.

Results:

Colorectal cancer and pseudomyxoma had the highest sensitivity to rMETase. Pancreatic and ovarian cancer also responded to rMETase, but to a lesser degree.

Conclusion:

Patients with tumors with at least 40% sensitivity to rMETase in the HDRA are being considered as candidates for methionine restriction therapy, which includes the use of rMETase in combination with a low-methionine diet.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Cancer Diagn Progn Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Cancer Diagn Progn Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos