Lysophosphatidic acid as a potential biomarker for ovarian and other gynecologic cancers

被引:536
作者
Xu, Y
Shen, ZZ
Wiper, DW
Wu, MZ
Morton, RE
Elson, P
Kennedy, AW
Belinson, J
Markman, M
Casey, G
机构
[1] Cleveland Clin Fdn, Dept Gynecol & Obstet, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Cell Biol, Cleveland, OH 44195 USA
[3] Cleveland Clin Fdn, Dept Biostat, Cleveland, OH 44195 USA
[4] Cleveland Clin Fdn, Ctr Canc, Cleveland, OH 44195 USA
[5] Cleveland State Univ, Dept Chem, Cleveland, OH 44115 USA
[6] Cleveland Clin Fdn, Dept Canc Biol, Cleveland, OH 44195 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1998年 / 280卷 / 08期
关键词
D O I
10.1001/jama.280.8.719
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context.-Lysophosphatidic acid (LPA) has been shown to stimulate proliferation of ovarian cancer cells and is present in the ascitic fluid of patients with ovarian cancer. Objectives.-To determine whether elevated levels of LPA are present in plasma from patients with ovarian cancer and other gynecologic malignancies compared with healthy controls and to evaluate whether an elevated LPA plasma level may be a biomarker for these diseases. Design.-A research assay was used to measure total LPA levels in plasma from healthy women and women with different diseases. All LPA assays and comparison of LPA levels and CA125 tan ovarian cancer biomarker) levels were performed by observers blinded to patient status or group. Setting.-The Cleveland Clinic Foundation. Participants.-A convenience sample of 48 healthy control women, 48 women with ovarian cancer, 36 women with other gynecologic cancers, 17 women with benign gynecologic diseases, 11 women with breast cancer, and 5 women with leukemias. Main Outcome Measures.-Total LPA levels in plasma Samples from patients and controls. Results.-Patients in the ovarian cancer group had significantly higher plasma LPA levels (mean, 8.6 mu mol/L; range, 1.0-43.1 mu mol/L) compared with the healthy control group (mean, 0.6 mu mol/L; range, <0.1-6.3 mu mol/L) (P<.001). Elevated plasma LPA levels were detected in 9 of 10 patients with stage I ovarian cancer, 24 of 24 patients with stage 11, III, and IV ovarian cancer, and 14 of 14 patients with recurrent ovarian cancer. Of 36 patients with other gynecologic cancers, 33 also showed higher LPA levels (mean, 14.9 mu mol/L; range, <0.1-63.2 mu mol/L), compared with healthy controls (P<.001). Elevated plasma LPA levels were detected in 5 of 48 controls and 4 of 17 patients with benign gynecologic diseases and in no women with breast cancer or leukemia. In comparison, among a subset of patients with ovarian cancer, 28 of 47 had elevated CA125 levels, including 2 of 9 patients with stage I disease. Conclusions.-Plasma LPA levels may represent a potential biomarker for ovarian cancer and other gynecologic cancers. However, these findings are preliminary and require confirmation in larger studies.
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收藏
页码:719 / 723
页数:5
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