Fong K M, Zimmerman P V, Smith P J
Department of Pathology, University of Queensland Medical School, Herston, Australia.
Cancer Res. 1995 Jan 15;55(2):220-3.
We investigated the frequency and clinical significance of loss of heterozygosity (LOH) at the APC, MCC, and DCC tumor suppressor gene loci in 108 cases of resected non-small cell lung cancer (NSCLC). LOH at the APC/MCC gene cluster at chromosome 5q21 occurred frequently; it affected 29% of informative NSCLC cases and correlated with a significantly worse survival (P < 0.01). Furthermore, in the subtype most frequently affected (SCC), LOH at 5q not only correlated with a worse survival but also tumor involvement of the mediastinal and/or hilar nodes. In contrast, LOH at the DCC locus at chromosome 18q was far less frequent, occurring in 14% of NSCLC cases, and it was not associated with advanced stage or prognosis. These data suggest that LOH at 5q has a role in determining tumor progression and survival in NSCLC, and may prove to be a clinically useful prognostic indicator.
我们研究了108例手术切除的非小细胞肺癌(NSCLC)中,抑癌基因位点APC、MCC和DCC杂合性缺失(LOH)的频率及其临床意义。5号染色体q21处的APC/MCC基因簇频繁发生LOH;它影响了29%的信息性NSCLC病例,且与显著较差的生存率相关(P<0.01)。此外,在受影响最频繁的亚型(鳞状细胞癌)中,5号染色体的LOH不仅与较差的生存率相关,还与纵隔和/或肺门淋巴结的肿瘤累及相关。相比之下,18号染色体q处DCC位点的LOH频率要低得多,发生在14%的NSCLC病例中,且与晚期或预后无关。这些数据表明,5号染色体的LOH在决定NSCLC的肿瘤进展和生存中起作用,可能被证明是一种临床上有用的预后指标。