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比较总血浆溶血磷脂酸和血清 CA-125 作为上皮性卵巢癌诊断和随访的肿瘤标志物。

Comparison of total plasma lysophosphatidic acid and serum CA-125 as a tumor marker in the diagnosis and follow-up of patients with epithelial ovarian cancer.

机构信息

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Istanbul, Turkey.

出版信息

J Gynecol Oncol. 2010 Dec 30;21(4):248-54. doi: 10.3802/jgo.2010.21.4.248. Epub 2010 Dec 31.

DOI:10.3802/jgo.2010.21.4.248
PMID:21278887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3026304/
Abstract

OBJECTIVE

To evaluate the role of lysophosphatidic acid (LPA) as a tumor marker in diagnosis and follow-up of patients with epithelial ovarian cancer.

METHODS

Eighty-seven epithelial ovarian cancer patients, 74 benign ovarian tumor patients, and 50 healthy women were enrolled in the study. Twenty-nine of 87 epithelial ovarian cancer patients were followed up for 6 cycles of paclitaxel-carboplatin chemotherapy. CA-125 and total plasma LPA levels were measured preoperatively and before each chemotherapy cycle.

RESULTS

Preoperative total plasma LPA and serum CA-125 levels were significantly higher in patients with epithelial ovarian cancer compared to patients with benign ovarian tumors and healthy women. Cut-off value for LPA was determined as 1.3 µmol/L and sensitivity, specificity, positive predictive value and negative predictive value were 95%, 92%, 95% and 92%, respectively. Mean total plasma LPA level of 29 patients who received chemotherapy was 7.21±6.63 µmol/L preoperatively and 6.84±6.34 µmol/L, 6.34±5.92 µmol/L, 6.14±5.79 µmol/L, 5.86±5.68 µmol/L, 5.23±5.11 µmol/L and 5.21±5.32 µmol/L in measurements held just before the 1st, 2nd, 3rd, 4th, 5th and 6th chemotherapy cycles, respectively (ANOVA, p=0.832). Total plasma LPA levels decreased slightly with chemotherapy administration and there was a weak negative correlation (Spearman, r(s)=-0.151, p=0.034), compared to a significant negative correlation in CA-125 (Spearman, r(s)=-0.596, p<0.001).

CONCLUSION

LPA is a better biomarker for diagnosis of epithelial ovarian cancer compared to CA-125. However, measurement of total plasma LPA levels during chemotherapy administration have no superiority to the serum CA-125 levels.

摘要

目的

评估溶血磷脂酸(LPA)作为上皮性卵巢癌诊断和随访肿瘤标志物的作用。

方法

研究纳入 87 例上皮性卵巢癌患者、74 例良性卵巢肿瘤患者和 50 例健康女性。87 例上皮性卵巢癌患者中有 29 例接受紫杉醇联合卡铂化疗 6 个周期,分别在术前和每个化疗周期前检测 CA-125 和总血浆 LPA 水平。

结果

上皮性卵巢癌患者术前总血浆 LPA 和血清 CA-125 水平明显高于良性卵巢肿瘤患者和健康女性。LPA 的截断值为 1.3 μmol/L,灵敏度、特异性、阳性预测值和阴性预测值分别为 95%、92%、95%和 92%。接受化疗的 29 例患者的平均总血浆 LPA 水平分别为术前 7.21±6.63 μmol/L、化疗前第 1、2、3、4、5、6 个周期的 6.84±6.34 μmol/L、6.34±5.92 μmol/L、6.14±5.79 μmol/L、5.86±5.68 μmol/L、5.23±5.11 μmol/L 和 5.21±5.32 μmol/L(方差分析,p=0.832)。随着化疗的进行,总血浆 LPA 水平略有下降,与 CA-125 呈弱负相关(Spearman,r(s)=-0.151,p=0.034),而与 CA-125 呈显著负相关(Spearman,r(s)=-0.596,p<0.001)。

结论

与 CA-125 相比,LPA 是上皮性卵巢癌诊断的更好的生物标志物。然而,在化疗期间测量总血浆 LPA 水平并没有优于血清 CA-125 水平。

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本文引用的文献

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Lysophosphatidic acid: an ovarian cancer marker.溶血磷脂酸:一种卵巢癌标志物。
Eur J Gynaecol Oncol. 2008;29(5):511-4.
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Lysophosphatidic acid receptors determine tumorigenicity and aggressiveness of ovarian cancer cells.溶血磷脂酸受体决定卵巢癌细胞的致瘤性和侵袭性。
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Carba analogs of cyclic phosphatidic acid are selective inhibitors of autotaxin and cancer cell invasion and metastasis.环磷酸酯的碳类似物是自分泌运动因子以及癌细胞侵袭和转移的选择性抑制剂。
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Lysophosphatidic acid is constitutively produced by human peritoneal mesothelial cells and enhances adhesion, migration, and invasion of ovarian cancer cells.溶血磷脂酸由人腹膜间皮细胞组成性产生,并增强卵巢癌细胞的黏附、迁移和侵袭能力。
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Cyclooxygenase-2 functions as a downstream mediator of lysophosphatidic acid to promote aggressive behavior in ovarian carcinoma cells.环氧化酶-2作为溶血磷脂酸的下游介质,促进卵巢癌细胞的侵袭行为。
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Role of phospholipase D in agonist-stimulated lysophosphatidic acid synthesis by ovarian cancer cells.磷脂酶D在卵巢癌细胞激动剂刺激的溶血磷脂酸合成中的作用。
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