Taback Bret, Bilchik Anton J, Saha Sukamal, Nakayama Takahiro, Wiese David A, Turner Roderick R, Kuo Christine T, Hoon Dave S B
Department of Molecular Oncology, John Wayne Cancer Institute, Saint John's Health Center, Santa Monica, CA 90404, USA.
Int J Cancer. 2004 Sep 1;111(3):409-14. doi: 10.1002/ijc.20268.
Inaccurate staging of colorectal cancer (CRC) has been attributed to the failure to detect lymph node metastases by conventional pathology. We have previously reported the use of lymphatic mapping to accurately identify those lymph nodes most likely to harbor micrometastatic disease and permit focused pathologic examination. Mutation of K-ras allele at codons 12 or 13 occurs frequently in early stages of CRC development. The purpose of our study was to assess sentinel lymph nodes (SLN) for occult CRC micrometastases using a unique peptide nucleic acid (PNA) clamp PCR assay specific for K-ras mutations. Seventy-two paraffin-embedded primary CRC and paired SLN were evaluated by PNA clamp PCR for K-ras mutations. Thirty primary tumors (42%) were positive for K-ras mutations, and in 5 of these cases the SLN were positive for metastases by Hematoxylin and Eosin staining. PNA clamp PCR identified occult metastases in an additional 6 patients, upstaging 24% of K-ras positive primary CRCs (p = 0.014). No K-ras mutations were detected among the 20 noncancer lymph nodes assessed. This study demonstrates the utility, specificity and sensitivity of PNA clamp PCR assay in identifying occult micrometastases in the SLN of CRC patients by single-base mutation analysis.
结直肠癌(CRC)分期不准确被认为是传统病理学未能检测到淋巴结转移所致。我们之前报道过利用淋巴绘图来准确识别那些最有可能隐匿微转移疾病的淋巴结,并进行有针对性的病理检查。K-ras基因第12或13密码子的突变在CRC发展的早期阶段经常出现。我们研究的目的是使用一种针对K-ras突变的独特肽核酸(PNA)钳夹PCR检测法来评估前哨淋巴结(SLN)是否存在隐匿性CRC微转移。通过PNA钳夹PCR对72例石蜡包埋的原发性CRC及配对的SLN进行K-ras突变评估。30例原发性肿瘤(42%)K-ras突变呈阳性,其中5例的SLN经苏木精和伊红染色显示转移呈阳性。PNA钳夹PCR在另外6例患者中检测到隐匿性转移,使24%的K-ras阳性原发性CRC分期上调(p = 0.014)。在评估的20个非癌性淋巴结中未检测到K-ras突变。本研究证明了PNA钳夹PCR检测法通过单碱基突变分析在识别CRC患者SLN隐匿性微转移方面的实用性、特异性和敏感性。