1.The Impact of Cigarette Smoking on the Frequency of and Qualitative Differences in KRAS Mutations in Korean Patients with Lung Adenocarcinoma.
Hye Ryun KIM ; Jung Ryun AHN ; Jin Gu LEE ; Doo Hee BANG ; Sang Jun HA ; Yun Kyoung HONG ; Sun Mi KIM ; Ki Chang NAM ; Sun Young RHA ; Ross A SOO ; Gregory J RIELY ; Joo Hang KIM ; Byoung Chul CHO
Yonsei Medical Journal 2013;54(4):865-874
PURPOSE: This study was designed to determine the relationship of cigarette smoking to the frequency and qualitative differences among KRAS mutations in lung adenocarcinomas from Korean patients. MATERIALS AND METHODS: Detailed smoking histories were obtained from 200 consecutively enrolled patients with lung adenocarcinoma according to a standard protocol. EGFR (exons 18 to 21) and KRAS (codons 12/13) mutations were determined via direct-sequencing. RESULTS: The incidence of KRAS mutations was 8% (16 of 200) in patients with lung adenocarcinoma. KRAS mutations were found in 5.8% (7 of 120) of tumors from never-smokers, 15% (6 of 40) from former-smokers, and 7.5% (3 of 40) from current-smokers. The frequency of KRAS mutations did not differ significantly according to smoking history (p=0.435). Never-smokers were significantly more likely than former or current smokers to have a transition mutation (G-->A or C-->T) rather than a transversion mutation (G-->T or G-->C) that is known to be smoking-related (p=0.011). In a Cox regression model, the adjusted hazard ratios for the risk of progression with epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) were 0.24 (95% CI, 0.14-0.42; p<0.001) for the EGFR mutation and 1.27 (95% CI, 0.58-2.79; p=0.537) for the KRAS mutation. CONCLUSION: Cigarette smoking did not influence the frequency of KRAS mutations in lung adenocarcinomas in Korean patients, but influenced qualitative differences in the KRAS mutations.
Adenocarcinoma/drug therapy/etiology/*genetics/pathology
;
Adult
;
Aged
;
Aged, 80 and over
;
Asian Continental Ancestry Group/genetics
;
Female
;
Humans
;
Incidence
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Lung Neoplasms/drug therapy/etiology/*genetics/pathology
;
Male
;
Middle Aged
;
*Mutation
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Mutation Rate
;
Proportional Hazards Models
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Proto-Oncogene Proteins/*genetics
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Receptor, Epidermal Growth Factor/antagonists & inhibitors/genetics
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Smoking/adverse effects/*genetics
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Treatment Outcome
;
ras Proteins/*genetics
2.Colorectal adenocarcinoma as a second malignant neoplasm following rhabdomyosarcoma of the urinary bladder: a case report.
Sung Shin PARK ; Byoung Kwon KIM ; Chong Jai KIM ; Woo Sun KIM ; In One KIM ; Kwi Won PARK ; Hee Young SHIN ; Hyo Seop AHN
Journal of Korean Medical Science 2000;15(4):475-477
Following improvements in therapy for childhood malignancies, the striking increase in survival rate over the past 30 years has led to the increase risk of developing second malignant neoplasms (SMNs). We report a case of colorectal carcinoma as a SMN, following treatment for rhabdomyosarcoma. The patient was diagnosed with rhabdomyosarcoma of the urinary bladder at his age of three years, and developed adenocarcinoma in the colon 13 years later. Histologic examination of the surgical specimen revealed adenocarcinoma involving the rectosigmoid area with radiation colitis in its background. The tumor cells showed strong immunoreactivity for p53 protein, suggesting the role of irradiation and p53 mutation in carcinogenesis. This case emphasizes the need for dose observation in survivors of early childhood malignancies treated with radiation and multiagent chemotherapy.
Adenocarcinoma/pathology
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Adenocarcinoma/genetics
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Adenocarcinoma/etiology+ACo-
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Adolescence
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Antineoplastic Agents, Combined/therapeutic use
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Antineoplastic Agents, Combined/adverse effects+ACo-
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Bladder Neoplasms+ACo-/radiotherapy
;
Bladder Neoplasms+ACo-/drug therapy
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Case Report
;
Colitis/pathology
;
Colitis/etiology
;
Colorectal Neoplasms/pathology
;
Colorectal Neoplasms/genetics
;
Colorectal Neoplasms/etiology+ACo-
;
Combined Modality Therapy
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Cyclophosphamide/adverse effects
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Cyclophosphamide/administration +ACY- dosage
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Doxorubicin/adverse effects
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Doxorubicin/administration +ACY- dosage
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Genes, p53
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Human
;
Male
;
Neoplasm Proteins/analysis
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Neoplasms, Radiation-Induced/pathology
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Neoplasms, Radiation-Induced/genetics
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Neoplasms, Radiation-Induced/etiology+ACo-
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Neoplasms, Second Primary/etiology+ACo-
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Protein p53/analysis
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Radiation Injuries/pathology
;
Radiation Injuries/etiology
;
Radiotherapy/adverse effects+ACo-
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Rhabdomyosarcoma+ACo-/radiotherapy
;
Rhabdomyosarcoma+ACo-/drug therapy
;
Sigmoid Neoplasms/pathology
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Sigmoid Neoplasms/genetics
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Sigmoid Neoplasms/etiology
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Time Factors
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Vincristine/adverse effects
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Vincristine/administration +ACY- dosage
3.Colorectal adenocarcinoma as a second malignant neoplasm following rhabdomyosarcoma of the urinary bladder: a case report.
Sung Shin PARK ; Byoung Kwon KIM ; Chong Jai KIM ; Woo Sun KIM ; In One KIM ; Kwi Won PARK ; Hee Young SHIN ; Hyo Seop AHN
Journal of Korean Medical Science 2000;15(4):475-477
Following improvements in therapy for childhood malignancies, the striking increase in survival rate over the past 30 years has led to the increase risk of developing second malignant neoplasms (SMNs). We report a case of colorectal carcinoma as a SMN, following treatment for rhabdomyosarcoma. The patient was diagnosed with rhabdomyosarcoma of the urinary bladder at his age of three years, and developed adenocarcinoma in the colon 13 years later. Histologic examination of the surgical specimen revealed adenocarcinoma involving the rectosigmoid area with radiation colitis in its background. The tumor cells showed strong immunoreactivity for p53 protein, suggesting the role of irradiation and p53 mutation in carcinogenesis. This case emphasizes the need for dose observation in survivors of early childhood malignancies treated with radiation and multiagent chemotherapy.
Adenocarcinoma/pathology
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Adenocarcinoma/genetics
;
Adenocarcinoma/etiology+ACo-
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Adolescence
;
Antineoplastic Agents, Combined/therapeutic use
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Antineoplastic Agents, Combined/adverse effects+ACo-
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Bladder Neoplasms+ACo-/radiotherapy
;
Bladder Neoplasms+ACo-/drug therapy
;
Case Report
;
Colitis/pathology
;
Colitis/etiology
;
Colorectal Neoplasms/pathology
;
Colorectal Neoplasms/genetics
;
Colorectal Neoplasms/etiology+ACo-
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Combined Modality Therapy
;
Cyclophosphamide/adverse effects
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Cyclophosphamide/administration +ACY- dosage
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Doxorubicin/adverse effects
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Doxorubicin/administration +ACY- dosage
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Genes, p53
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Human
;
Male
;
Neoplasm Proteins/analysis
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Neoplasms, Radiation-Induced/pathology
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Neoplasms, Radiation-Induced/genetics
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Neoplasms, Radiation-Induced/etiology+ACo-
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Neoplasms, Second Primary/etiology+ACo-
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Protein p53/analysis
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Radiation Injuries/pathology
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Radiation Injuries/etiology
;
Radiotherapy/adverse effects+ACo-
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Rhabdomyosarcoma+ACo-/radiotherapy
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Rhabdomyosarcoma+ACo-/drug therapy
;
Sigmoid Neoplasms/pathology
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Sigmoid Neoplasms/genetics
;
Sigmoid Neoplasms/etiology
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Time Factors
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Vincristine/adverse effects
;
Vincristine/administration +ACY- dosage
4.The advancement of predictive diagnosis and molecular mechanism in multiple primary lung cancer.
Lan YUAN ; Lun-Xu LIU ; Guo-Wei CHE
Chinese Journal of Cancer 2010;29(5):575-578
Due to the advanced diagnostic technique and better understanding for multiple primary lung cancers (MPLC), the increasing incidence of MPLC has been reported. Very often, MPLC are misdiagnosed as metastasis because of lacking efficient molecular biomarkers for prediction and diagnosis. Studies on the molecular mechanism for tumorgenesis and progression of MPLC may therefore facilitate the discovery of biomarkers for disease diagnosis and prognosis, so that an individual and rational treatment can be achieved. We tried to further our understanding and improve the diagnostic skill for MPLC by reviewing the current status and the latest advancement of molecular markers related to MPLC.
Adenocarcinoma
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pathology
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Biomarkers, Tumor
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analysis
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Carcinoma, Non-Small-Cell Lung
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drug therapy
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radiotherapy
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Carcinoma, Small Cell
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pathology
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Carcinoma, Squamous Cell
;
pathology
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Chromosome Deletion
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DNA Damage
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Genes, Tumor Suppressor
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Humans
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Incidence
;
Lung Neoplasms
;
diagnosis
;
epidemiology
;
etiology
;
genetics
;
Neoplasms, Multiple Primary
;
diagnosis
;
epidemiology
;
etiology
;
genetics
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Smoking
;
adverse effects