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Japanese Journal of Cancer Research : Gann logoLink to Japanese Journal of Cancer Research : Gann
. 1996 Jun;87(6):650–654. doi: 10.1111/j.1349-7006.1996.tb00272.x

Detection of Gastric Cancer Micrometastases in Lymph Nodes by Amplification of Keratin 19 mRNA with Reverse Transcriptase‐Polymerase Chain Reaction

Sbinzaburo Noguchi 1,, Masahiro Hiratsuka 1, Hiroshi Furukawa 1, Tomohiko Aihara 1, Tsutomu Kasugai 1, Sumihito Tamura 1, Shingi Imaoka 1, Hiroki Koyama 1, Takeshi Iwanaga 1
PMCID: PMC5921146  PMID: 8766530

Abstract

A sensitive method for the detection of gastric cancer micrometastases in lymph nodes was developed. The method was based on amplification of keratin 19 mRNA by reverse transcriptase‐polymerase chain reaction (RT‐PCR). Keratin 19 RT‐PCR showed that keratin 19 mRNA was expressed in all 12 gastric cancers, but not in any of 20 normal control lymph nodes, indicating that keratin 19 mRNA is a good target of RT‐PCR for the detection of gastric cancer micrometastases in lymph nodes. Serial dilution studies of RNA extracted from gastric cancers against RNA extracted from control lymph nodes demonstrated that the detection sensitivity of the keratin 19 RT‐PCR method was one cancer cell in 103‐105 lymph node cells. Detectability of lymph node metastases was compared between keratin 19 RT‐PCR and conventional histological examination, using 100 lymph nodes obtained from 12 gastric cancer patients. Keratin 19 mRNA was detected in all of the seven lymph nodes which were historically metastasis‐positive. Of the 93 lymph nodes which were histologically metastasisnegative, 79 were found not to express keratin 19 mRNA but 14 were found to express keratin 19 mRNA, indicating that these lymph nodes contained micrometastases which could not be detected by histological examination. These results demonstrate that keratin 19 RT‐PCR is a more sensitive method than histological examination for the detection of gastric micrometastases in lymph nodes.

Keywords: Gastric cancer, Micrometastasis, Lymph node, Keratin 19, RT‐PCR

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