Stanniocalcin-1 as a Novel Marker to Detect Minimal Residual Disease of Human Leukemia
YASUO TOHMIYA, YOSHIO KOIDE,1 SHINICHI FUJIMAKI,1 HIDEO HARIGAE,1 TADAO FUNATO,1 MITSUO KAKU,1 TOMONORI ISHII, YASUHIKO MUNAKATA, JUNICHI KAMEOKA and TAKESHI SASAKI
Department of Rheumatology and Hematology, 1Department of Molecular Diagnostics, Tohoku University Graduate School of Medicine, Sendai, Japan
Stanniocalcin is a glycoprotein hormone that regulates the calcium level in fish. We found that mRNA of human stanniocalcin 1 (STC-1) is detectable in phytohemagglutinin-stimulated T cells and in most human leukemia cell lines, suggesting a role of STC-1 for cell proliferation. This finding prompts us to study the usefulness of STC-1 for monitoring acute leukemia. The levels of STC-1 transcripts increased in patients with acute leukemia at diagnosis and relapse, as judged by quantitative real-time RT-PCR. Levels of transcripts rapidly decreased to within the cut-off levels, when the blast numbers decreased with chemotherapy. Prolonged elevation of STC-1 levels after treatment was associated with a poor prognosis. All of 7 patients relapsed 1 to 4 months after they showed an elevated level of the transcripts in clinical remission. These results indicate that STC-1 is a novel marker for minimal residual disease of acute leukemia, and for an early diagnosis of relapse.
keywords Stanniocalcin 1 (STC-1); leukemia; real-time PCR; minimal residual disease (MRD)
© 2004 Tohoku University Medical Press
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Tohoku J. Exp. Med., 2004, 204, 125-133
Address for reprints: Dr. Takeshi Sasaki, Department of Rheumatology and Hematology, Tohoku University Graduate School of Medicine, 1-1 Seiryomachi, Aoba-ku, Sendai 980-8574, Japan.
e-mail: takesa18@mail.tains.tohoku.ac.jp