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Clinical Cancer Research Vol. 10, 6544-6550, October 1, 2004
© 2004 American Association for Cancer Research


Molecular Oncology, Markers, Clinical Correlates

The Spermatozoa Protein, SLLP1, Is a Novel Cancer–Testis Antigen in Hematologic Malignancies

Zhiqing Wang1,2, Yana Zhang1,2, Arabinda Mandal3, Jian Zhang1,2, Francis J. Giles1,2, John C. Herr3 and Seah H. Lim1,2

1 Division of Hematology and Oncology, Texas Tech University Health Sciences Center, Amarillo, Texas; 2 Biotherapy and Stem Cell Transplant Program, Don and Sybil Harrington Cancer Center, Amarillo, Texas; and 3 Center for Research in Contraceptive and Reproductive Health, Department of Cell Biology, University of Virginia Health System, Charlottesville, Virginia

Purpose: Neoplastic cells often aberrantly express normal testicular proteins. Because these proteins have a very restricted normal tissue expression, they may be suitable targets for immunotherapy. SLLP1 is an intra-acrosomal, nonbacteriolytic, c lysozyme–like protein recently isolated from human spermatozoa. In this study, we determined whether SLLP1 is a novel cancer–testis antigen in hematologic malignancies

Experimental Design: SLLP1 expression in hematologic tumor cells and normal tissues was determined using a combination of reverse transcription-PCR, real-time PCR, and Western blot analysis. The presence of antibodies against SLLP1 was determined by ELISA analysis.

Results: SLLP1 was aberrantly expressed in the tumor cells from 2 of 9 acute myeloid leukemia, 3 of 11 chronic lymphocytic leukemia, 4 of 14 chronic myeloid leukemia, and 6 of 17 multiple myeloma. In contrast, they were not detected in corresponding specimens from any healthy donors. SLLP1 exhibited a very restricted normal tissue expression, being found only in testis/spermatozoa. SLLP1 was expressed in some tumor cells at a level of >25%. High titer IgG antibodies against SLLP1 were also detected in the sera of some of these patients.

Conclusions: SLLP1 is a novel cancer–testis antigen in hematologic malignancies and is capable of eliciting B-cell immune responses in vivo in cancer-bearing individuals. Our results, therefore, support SLLP1 as a protein target appropriate for additional in vitro study to define its suitability for immunotherapy.




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Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Cell Growth & Differentiation
Copyright © 2004 by the American Association for Cancer Research.