- Flow cytometric analysis of DNA ploidy in primary non-small cell carcinoma of the lung in Korea
-
Cheon SH, Sohn HY, Chang J, Kim SK, Ko EH, Kim SK, Lee WY, Lee DY, Shin DH, Jeong ET, Chung HT
- KMID: 1758501
- Yonsei Med J.
- 1993 Dec;34(4):365-370.
- doi: 10.3349/ymj.1993.34.4.365
Flow cytometrically determined nuclear DNA content has been measured on 74 formalin-fixed, paraffin embedded specimens of non-small cell carcinoma of the lung. Of the 60 tumors that were successfully analyzed,... -
- CITED
-
- Close
- SHARE
-
- Close
- Clinical Significance of Aberrant Wnt7a Promoter Methylation in Human Non-Small Cell Lung Cancer in Koreans
-
Kim TH, Moon JY, Kim SH, Paik SS, Yoon HJ, Shin DH, Park SS, Sohn JW
- KMID: 2129645
- J Korean Med Sci.
- 2015 Feb;30(2):155-161.
- doi: 10.3346/jkms.2015.30.2.155
The Wnt signaling pathway has regulatory roles in cell proliferation, differentiation, and polarity. Aberrant Wnt pathway regulation can lead to abnormal cell proliferation and cancer, and loss of Wnt7a expression... -
- CITED
-
- Close
- SHARE
-
- Close
- MiR-152 suppresses the proliferation and invasion of NSCLC cells by inhibiting FGF2
-
Cheng Z, Ma R, Tan W, Zhang L
- KMID: 2155377
- Exp Mol Med.
- 2014 Sep;46(9):e112.
- doi: 10.1038/emm.2014.51
MicroRNAs (miRNAs) regulate the proliferation and metastasis of cancer cells. Here, we showed that miR-152 was downregulated in non-small-cell lung cancer (NSCLC) tissues and cell lines. Overexpression of miR-152 suppressed... -
- CITED
-
- Close
- SHARE
-
- Close
- Letter to the Editor: Detection of EML4-ALK and Other ALK Fusion Genes in Lung Cancer: A Lesson from the Leukemia Fusion Gene Analysis and Future Application
-
Park TS, Jeon YL, Lee HJ, Jeong JH, Kim SY, Cho EH, Marschalek R, Meyer C
- KMID: 1372806
- J Korean Med Sci.
- 2012 May;27(5):576-577.
- doi: 10.3346/jkms.2012.27.5.576
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Epidermal Growth Factor Receptor Mutations and the Clinical Outcome in Male Smokers with Squamous Cell Carcinoma of Lung
-
Park SH, Ha SY, Lee JI, Lee H, Sim H, Kim YS, Hong J, Park J, Cho EK, Shin DB, Lee JH
- KMID: 1779162
- J Korean Med Sci.
- 2009 Jun;24(3):448-452.
- doi: 10.3346/jkms.2009.24.3.448
Epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer (NSCLC) have been reported to be related to certain clinical characteristics (i.e., female, non-smokers with adenocarcinoma) and gefitinib responsiveness.... -
- CITED
-
- Close
- SHARE
-
- Close
- Polymorphisms in Apoptosis-Related Genes and TP53 Mutations in Non-Small Cell Lung Cancer
-
Bae EY, Lee EJ, Kang HG, Lee SY, Jin G, Lee WK, Choi JE, Jeon HS, Lim JO, Lee EB, Park JY
- KMID: 1123458
- J Korean Med Sci.
- 2011 Nov;26(11):1527-1530.
- doi: 10.3346/jkms.2011.26.11.1527
Apoptosis plays an essential role in the elimination of mutated or transformed cells from the body. Therefore, polymorphisms of apoptosis-related genes may lead to an alteration in apoptotic capacity, thereby... -
- CITED
-
- Close
- SHARE
-
- Close
- Genetic Variants in the Wnt Signaling Pathway Are Not Associated with Survival Outcome of Non-Small Cell Lung Cancer in a Korean Population
-
Yoo SS, Hong MJ, Choi JE, Lee JH, Baek SA, Lee WK, Lee SY, Lee SY, Lee J, Cha SI, Kim CH, Cho S, Park JY
- KMID: 2363510
- J Korean Med Sci.
- 2016 Mar;31(3):463-466.
- doi: 10.3346/jkms.2016.31.3.463
Recently, genetic variants in the WNT signaling pathway have been reported to affect the survival outcome of Caucasian patients with early stage non-small cell lung cancer (NSCLC). We therefore attempted... -
- CITED
-
- Close
- SHARE
-
- Close
- Concomitance of P-gp/LRP Expression with EGFR Mutations in Exons 19 and 21 in Non-Small Cell Lung Cancers
-
Wei H, Lu W, Li M, Zhang Q, Lu S
- KMID: 2466351
- Yonsei Med J.
- 2016 Jan;57(1):50-57.
- doi: 10.3349/ymj.2016.57.1.50
PURPOSE: Traditional chemotherapy is the main adjuvant therapy for the treatment of non-small cell lung cancer (NSCLC). However, the emergence of multi-drug resistance (MDR) has greatly restricted the curative effect... -
- CITED
-
- Close
- SHARE
-
- Close
- Hypermethylation of p16(INK4a) in Korean Non-small Cell Lung Cancer Patients
-
Hong YS, Roh MS, Kim NY, Lee HJ, Kim HK, Lee KE, Kwak JY, Kim JY
- KMID: 1785786
- J Korean Med Sci.
- 2007 Sep;22(Suppl):S32-S37.
- doi: 10.3346/jkms.2007.22.S.S32
Promoter hypermethylation of the p16(INK4a) gene was investigated in 81 sets of samples of tumor tissue and adjacent normal tissue from Korean patients with primary lung cancer, using the modified... -
- CITED
-
- Close
- SHARE
-
- Close
- Comparative Quantification of Plasma hnRNP B1 mRNA in Non-small Cell Lung Cancer Patients by Real-time PCR
-
Kim JM, Hwang SH, Song EJ, Lee SY, Kim YD, Lee CH, Lee MK, Chang CL, Lee EY
- KMID: 1096978
- Korean J Lab Med.
- 2009 Jun;29(3):249-255.
- doi: 10.3343/kjlm.2009.29.3.249
BACKGROUND: Circulating cell-free nucleic acids are known to be a noninvasive diagnostic tool for cancer detection. Heterogeneous nuclear ribonucleoprotein (hnRNP) B1, a nuclear core complex, is overexpressed in early stage... -
- CITED
-
- Close
- SHARE
-
- Close
- Association Between MicroRNA196a2 rs11614913 Genotypes and the Risk of Non-Small Cell Lung Cancer in Korean Population
-
Hong YS, Kang HJ, Kwak JY, Park BL, You CH, Kim YM, Kim H
- KMID: 1093272
- J Prev Med Public Health.
- 2011 May;44(3):125-130.
- doi: 10.3961/jpmph.2011.44.3.125
OBJECTIVES: The microRNA (miRNA) miR-196a2 may play an important role in lung cancer development and survival by altering binding activity of target mRNA. In this study, we evaluated their associations... -
- CITED
-
- Close
- SHARE
-
- Close
- A Modified Extraction Method of Circulating Free DNA for Epidermal Growth Factor Receptor Mutation Analysis
-
Yuan H, Zhu ZZ, Lu Y, Liu F, Zhang W, Huang G, Zhu G, Jiang B
- KMID: 1779697
- Yonsei Med J.
- 2012 Jan;53(1):132-137.
- doi: 10.3349/ymj.2012.53.1.132
PURPOSE: Circulating free DNA (cfDNA) in plasma is promising to be a surrogate for tumor tissue DNA. However, not all epidermal growth factor receptor (EGFR) mutations in tumor tissue DNA... -
- CITED
-
- Close
- SHARE
-
- Close
