Gallagher Emma M, O'Shea Deirdre M, Fitzpatrick Patricia, Harrison Michèle, Gilmartin Breege, Watson Jenny A, Clarke Trevor, Leonard Martin O, McGoldrick Aloysius, Meehan Maria, Watson Chanel, Furlong Fiona, O'Kelly Patrick, Fitzpatrick John M, Dervan Peter A, O'Grady Anthony, Kay Elaine W, McCann Amanda
UCD School of Medicine and Medical Science, University College Dublin, Belfield, Dublin, Ireland.
Clin Cancer Res. 2008 Nov 1;14(21):6829-38. doi: 10.1158/1078-0432.CCR-08-0577.
This study documents the frequency of insulin-like growth factor-II (IGF-II) loss of imprinting (LOI) in a series of 87 bladder tissues. E-cadherin (CDH1) immunolocalization was also investigated due to the known redistribution of this adherence protein to the cytoplasm following exogenous exposure to IGF-II.
Informative IGF-II cases were identified following DNA-PCR amplification and subsequent sequencing of the transcribable ApaI RFLP in exon 9 of IGF-II. Similar approaches using primer-specific cDNA templates identified the imprinting status of IGF-II in these informative cases. CDH1 cellular localization was assessed on a tissue microarray platform of 114 urothelial carcinoma of the bladder (UCB) cases (70 pT(a) noninvasive and 44 pT(1) lamina propria invasive) using the commercially available Novocastra antibody.
IGF-II LOI was evident in 7 of 17 (41%) UCB tumors and 4 of 11 (36%) tumor-associated normal urothelial samples. Two of four pT(1) grade 3 tumors, the subject of much debate concerning their suitability for radical cystectomy, showed LOI at the IGF-II locus. In those tumors showing IGF-II LOI, 4 of 7 (57%) displayed concomitant CDH1 cytoplasmic staining. In contrast, only 3 of 10 (30%) IGF-II maintenance of imprinting tumors had concomitant CDH1 cytoplasmic localization. UCB cell lines displaying cytoplasmic CDH1 immunolocalization expressed significantly higher levels of IGF-II (CAL29, HT1376, and RT112) compared with RT4, a cell line displaying crisp membranous CDH1 staining. Finally, cytoplasmic CDH1 staining was an independent predictor of a shorter time to recurrence independent of tumor grade and stage.
We suggest that CDH1 cytoplasmic immunolocalization as a result of increased IGF-II levels identifies those nonmuscle invasive presentations most likely to recur and therefore might benefit from more radical nonconserving bladder surgery.
本研究记录了87例膀胱组织中胰岛素样生长因子-II(IGF-II)印记缺失(LOI)的频率。由于已知外源性暴露于IGF-II后这种黏附蛋白会重新分布到细胞质中,因此还研究了E-钙黏蛋白(CDH1)的免疫定位。
通过DNA-PCR扩增以及随后对IGF-II第9外显子中可转录的ApaI限制性片段长度多态性(RFLP)进行测序,确定了具有信息性的IGF-II病例。在这些具有信息性的病例中,使用引物特异性cDNA模板的类似方法确定了IGF-II的印记状态。使用市售的诺华卡斯尔抗体,在114例膀胱尿路上皮癌(UCB)病例(70例pT(a)非侵袭性和44例pT(1)固有层侵袭性)的组织微阵列平台上评估了CDH1的细胞定位。
在17例UCB肿瘤中的7例(41%)和11例肿瘤相关正常尿路上皮样本中的4例(36%)中,IGF-II LOI明显。在4例pT(1) 3级肿瘤中,有2例在IGF-II基因座显示LOI,这2例肿瘤对于是否适合进行根治性膀胱切除术存在很多争议。在那些显示IGF-II LOI的肿瘤中,7例中有4例(57%)同时出现CDH1细胞质染色。相比之下,在10例维持IGF-II印记的肿瘤中,只有3例(30%)同时出现CDH1细胞质定位。与显示清晰膜性CDH1染色的RT4细胞系相比,显示细胞质CDH1免疫定位的UCB细胞系(CAL29、HT1376和RT112)表达的IGF-II水平明显更高。最后,细胞质CDH1染色是独立于肿瘤分级和分期的复发时间较短的预测指标。
我们认为,由于IGF-II水平升高导致的CDH1细胞质免疫定位可识别出最有可能复发的非肌肉侵袭性表现,因此可能受益于更激进的非保留性膀胱手术。