Lee Shin Yup, Jeon Hyo-Sung, Hwangbo Yup, Jeong Ji Yun, Park Ji Young, Lee Eun Jin, Jin Guang, Shin Kyung Min, Yoo Seung Soo, Lee Jaehee, Lee Eung Bae, Cha Seung Ick, Kim Chang Ho, Park Jae Yong
Department of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Korea.
Mol Carcinog. 2015 Feb;54(2):93-101. doi: 10.1002/mc.22077. Epub 2013 Sep 4.
A large number of studies have evaluated the impact of TP53 mutations on the prognosis of patients with non-small cell lung cancer (NSCLC); however, the results of these studies are still controversial. Recently, considerable intratumor heterogeneity for genetic alterations has been demonstrated in various human cancers, including lung cancer. In the present study, we evaluated TP53 mutations in NSCLCs by direct sequencing and observed remarkable variation in the values of relative intensity (RI, the height of the peak of mutated allele/the height of the peak of non-mutated allele) of the mutations. We also examined whether the RI values were associated with intratumor heterogeneity of TP53 mutations. In addition, we evaluated the relationship between TP53 mutations and survival outcome. The patients with a TP53 mutation did not have significantly worse survival compared to those without the mutation. However, when tumors with a TP53 mutation were categorized into two groups, those with a low and those with a high RI, the latter group had significantly worse survival compared to those with wild-type TP53 (adjusted hazard ratio = 2.58, 95% confidence interval = 1.21-5.48, P = 0.01), whereas the former group did not. These results suggest that intratumor genetic heterogeneity may be an important factor in determining the role of TP53 mutations on the prognosis of NSCLC patients.
大量研究评估了TP53突变对非小细胞肺癌(NSCLC)患者预后的影响;然而,这些研究结果仍存在争议。最近,在包括肺癌在内的各种人类癌症中已证实存在显著的肿瘤内基因改变异质性。在本研究中,我们通过直接测序评估了NSCLC中的TP53突变,并观察到这些突变的相对强度(RI,突变等位基因峰高/非突变等位基因峰高)值存在显著差异。我们还研究了RI值是否与TP53突变的肿瘤内异质性相关。此外,我们评估了TP53突变与生存结果之间的关系。与未发生TP53突变的患者相比,发生TP53突变的患者生存率并没有显著更差。然而,当将发生TP53突变的肿瘤分为两组,即RI值低的组和RI值高的组时,与野生型TP53患者相比,后一组的生存率显著更差(校正风险比=2.58,95%置信区间=1.21-5.48,P=0.01),而前一组则没有。这些结果表明,肿瘤内基因异质性可能是决定TP53突变对NSCLC患者预后作用的一个重要因素。