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循环前列腺肿瘤细胞的灵敏巢式逆转录聚合酶链反应检测:基于前列腺特异性膜抗原和前列腺特异性抗原检测的比较

Sensitive nested reverse transcription polymerase chain reaction detection of circulating prostatic tumor cells: comparison of prostate-specific membrane antigen and prostate-specific antigen-based assays.

作者信息

Israeli R S, Miller W H, Su S L, Powell C T, Fair W R, Samadi D S, Huryk R F, DeBlasio A, Edwards E T, Wise G J

机构信息

Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.

出版信息

Cancer Res. 1994 Dec 15;54(24):6306-10.

PMID:7527294
Abstract

A highly sensitive nested reverse transcriptase-PCR assay, with primers derived from the prostate-specific antigen (PSA) and prostate-specific membrane antigen (PSM) cDNA sequences, has been used to detect occult hematogenous micrometastatic prostate cells. In 77 patients with prostate cancer, PSM and PSA primers detected circulating prostate cells in 48 (62.3%) and 7 (9.1%) patients, respectively. In treated stage D disease patients, PSM primers detected cells in 16 of 24 patients (66.7%), while PSA primers detected cells in 6 of 24 (25%). In post-radical prostectomy patients with negative serum PSA values, PSM primers detected metastases in 21 of 31 patients (67.7%), whereas PSA primers detected cells in only 1 of 33 (3.0%), indicating that micrometastatic spread may be a relatively early event in prostate cancer. The analysis of 40 individuals without known prostate cancer provides evidence that this assay is highly specific and suggests that PSM expression may predict the development of cancer in patients without clinically apparent prostate cancer. Using PSM primers, we detected micrometastases in 4 of 40 controls, 2 of whom had known benign prostatic hyperplasia and were later found to have previously undetected prostate cancer. The clinical significance of detection of hematogenous micrometastic prostate cells using PSM primers and potential applications of this molecular assay, as well as the assay for PSA, merit further study.

摘要

一种高度灵敏的巢式逆转录聚合酶链反应检测方法,其引物源自前列腺特异性抗原(PSA)和前列腺特异性膜抗原(PSM)的cDNA序列,已被用于检测隐匿性血行微转移前列腺细胞。在77例前列腺癌患者中,PSM引物和PSA引物分别在48例(62.3%)和7例(9.1%)患者中检测到循环前列腺细胞。在接受治疗的D期疾病患者中,PSM引物在24例患者中的16例(66.7%)检测到细胞,而PSA引物在24例中的6例(25%)检测到细胞。在血清PSA值为阴性的根治性前列腺切除术后患者中,PSM引物在31例患者中的21例(67.7%)检测到转移灶,而PSA引物仅在33例中的1例(3.0%)检测到细胞,这表明微转移扩散可能是前列腺癌中相对较早发生的事件。对40例无已知前列腺癌的个体进行分析表明,该检测方法具有高度特异性,并提示PSM表达可能预测无临床明显前列腺癌患者的癌症发展。使用PSM引物,我们在40例对照中的4例检测到微转移,其中2例已知患有良性前列腺增生,后来发现患有先前未检测到的前列腺癌。使用PSM引物检测血行微转移前列腺细胞的临床意义以及该分子检测方法和PSA检测方法的潜在应用值得进一步研究。

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