Dhillo Waljit S, Savage Philip, Murphy Kevin G, Chaudhri Owais B, Patterson Michael, Nijher Gurjinder M, Foggo Vanessa M, Dancey Garin S, Mitchell Hugh, Seckl Michael J, Ghatei Mohammad A, Bloom Stephen R
Department of Metabolic Medicine, Hammersmith Hospital, Imperial College London, London, W12 ONN, UK.
Am J Physiol Endocrinol Metab. 2006 Nov;291(5):E878-84. doi: 10.1152/ajpendo.00555.2005. Epub 2006 Jun 6.
Kisspeptin is a 54-amino acid peptide, encoded by the anti-metastasis gene KiSS-1, that activates G protein-coupled receptor 54 (GPR54). The kisspeptin-GPR54 system is critical to normal reproductive development. KiSS-1 gene expression is increased in the human placenta in normal and molar pregnancies. Circulating kisspeptin is dramatically increased in normal pregnancy, but levels in GTN have not previously been reported. The present study was designed to determine whether plasma kisspeptin levels are altered in patients with malignant GTN. Thirty-nine blood samples were taken from 11 patients with malignant GTN at presentation during and after chemotherapy. Blood was also sampled from nonpregnant and pregnant volunteers. Plasma kisspeptin IR and hCG concentrations were measured. Plasma kisspeptin IR concentration in nonpregnant (n = 16) females was <2 pmol/l. Plasma kisspeptin IR in females was 803 +/- 125 pmol/l in the first trimester of pregnancy (n = 13), 2,483 +/- 302 pmol/l in the third trimester of pregnancy (n = 7), and <2 pmol/l on day 15 postpartum (n = 7). Plasma kisspeptin IR and hCG concentrations in patients with malignant GTN were elevated at presentation and fell during and after treatment with chemotherapy in each patient (mean plasma kisspeptin IR: prechemotherapy 1,363 +/- 1,076 pmol/l vs. post-chemotherapy <2 pmol/l, P < 0.0001; mean plasma hCG: prechemotherapy 227,191 +/- 152,354 U/l vs. postchemotherapy 2 U/l, P < 0.0001). Plasma kisspeptin IR strongly positively correlated with plasma hCG levels (r(2) = 0.99, P < 0.0001). Our results suggest that measurement of plasma kisspeptin IR may be a novel tumor marker in patients with malignant GTN.
kisspeptin是一种由抗转移基因KiSS-1编码的含54个氨基酸的肽,它可激活G蛋白偶联受体54(GPR54)。kisspeptin-GPR54系统对正常生殖发育至关重要。在正常妊娠和葡萄胎妊娠中,人胎盘中KiSS-1基因表达增加。正常妊娠时循环中的kisspeptin显著升高,但此前尚未报道妊娠滋养细胞肿瘤(GTN)患者的水平。本研究旨在确定恶性GTN患者血浆中kisspeptin水平是否发生改变。在化疗期间及化疗后,从11例恶性GTN患者就诊时采集了39份血样。还从非妊娠和妊娠志愿者中采集了血样。检测血浆中kisspeptin免疫反应性(IR)和人绒毛膜促性腺激素(hCG)浓度。非妊娠女性(n = 16)血浆中kisspeptin IR浓度<2 pmol/L。妊娠早期女性(n = 13)血浆中kisspeptin IR为803±125 pmol/L,妊娠晚期(n = 7)为2483±302 pmol/L,产后第15天(n = 7)<2 pmol/L。恶性GTN患者就诊时血浆中kisspeptin IR和hCG浓度升高,化疗期间及化疗后每位患者的水平均下降(血浆kisspeptin IR平均值:化疗前1363±1076 pmol/L vs化疗后<2 pmol/L,P<0.0001;血浆hCG平均值:化疗前227191±152354 U/L vs化疗后2 U/L,P<0.0001)。血浆中kisspeptin IR与血浆hCG水平呈强正相关(r² = 0.99,P<0.0001)。我们的结果表明,检测血浆中kisspeptin IR可能是恶性GTN患者一种新的肿瘤标志物。