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      KCI등재 SCIE SCOPUS

      Prevalence of p16 Methylation and Prognostic Factors in Plasma Cell Myeloma at a Single Institution in Korea

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      https://www.riss.kr/link?id=A101631648

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      다국어 초록 (Multilingual Abstract)

      Background: The primary purpose of this study was to investigate the prevalence and characteristics of p16 methylation and determine the prognostic implications of the clinical data, hematologic data, and p16 methylation changes in plasma cell myeloma...

      Background: The primary purpose of this study was to investigate the prevalence and characteristics of p16 methylation and determine the prognostic implications of the clinical data, hematologic data, and p16 methylation changes in plasma cell myeloma (PCM). Methods: We reviewed clinical characteristics and results of laboratory tests and investigated the response to combination chemotherapy and survival time. DNA methylation of the p16 gene was tested by methylation-specific PCR. Clinical significance was evaluated. Results: A total of 103 patients were enrolled in this study. The median patient age was 59.0 yr at diagnosis and the male to female ratio was 1.15:1. According to the International Staging System (ISS), patients were diagnosed as stage: I (N=17, 16.5%), II (N=41, 39.8%), III (N=39, 37.9%), or not classified (N=6). Forty-five (43.7%) patients and 36 (35.0%) patients showed abnormal karyotype and complex karyotype, respectively, on the chromosome study. The p16 methylation was observed in 39 (37.9%) of 103 patients, but there was no significant association between p16 methylation status and other clinical or laboratory factors and survival outcome. Male gender, albumin, and complex karyotype were independent prognostic factors for overall survival according to multivariate analysis (P <0.05). Conclusions: The male gender, low serum albumin level, and complex karyotype were independent poor prognostic factors for PCM. p16 methylation was relatively common in PCM,but did not influence the survival outcome.

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      참고문헌 (Reference)

      1 Guillerm G, "p16INK4a and p15INK4b gene methylations in plasma cells from monoclonal gammopathy of undetermined significance" 98 : 244-246, 2001

      2 Ribas C, "p16 gene methylation lacks correlation with angiogenesis and prognosis in multiple myeloma" 222 : 247-254, 2005

      3 Gonzalez-Paz N, "Tumor suppressor p16 methylation in multiple myeloma: biological and clinical implications" 109 : 1228-1232, 2007

      4 Ries LAG MD KM, "SEER Cancer Statistics Review" National Cancer Institute

      5 Ohashi H, "Relationship between methylation of the p15 gene and ectopic expression of the EVI-1 gene in myelodysplastic syndromes (MDS)" 15 : 990-991, 2001

      6 Bladé J, "Prognostic factors for multiple myeloma in the era of novel agents" 19 (19): 7117-7120, 2008

      7 Dominguez G, "Prevalence of aberrant methylation of p14ARF over p16INK4a in some human primary tumors" 530 : 9-17, 2003

      8 Shiraz OB, "Possible down regulation of the p16 gene promoter in individuals with hepatocellular carcinoma" 11 : 719-723, 2011

      9 McKenna RW, "Plasma cell neoplasm, In WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th ed" IARC 200-213, 2008

      10 Harousseau JL, "Multiple myeloma: ESMO clinical recommendations for diagnosis, treatment and follow-up" 19 (19): 255-257, 2008

      1 Guillerm G, "p16INK4a and p15INK4b gene methylations in plasma cells from monoclonal gammopathy of undetermined significance" 98 : 244-246, 2001

      2 Ribas C, "p16 gene methylation lacks correlation with angiogenesis and prognosis in multiple myeloma" 222 : 247-254, 2005

      3 Gonzalez-Paz N, "Tumor suppressor p16 methylation in multiple myeloma: biological and clinical implications" 109 : 1228-1232, 2007

      4 Ries LAG MD KM, "SEER Cancer Statistics Review" National Cancer Institute

      5 Ohashi H, "Relationship between methylation of the p15 gene and ectopic expression of the EVI-1 gene in myelodysplastic syndromes (MDS)" 15 : 990-991, 2001

      6 Bladé J, "Prognostic factors for multiple myeloma in the era of novel agents" 19 (19): 7117-7120, 2008

      7 Dominguez G, "Prevalence of aberrant methylation of p14ARF over p16INK4a in some human primary tumors" 530 : 9-17, 2003

      8 Shiraz OB, "Possible down regulation of the p16 gene promoter in individuals with hepatocellular carcinoma" 11 : 719-723, 2011

      9 McKenna RW, "Plasma cell neoplasm, In WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th ed" IARC 200-213, 2008

      10 Harousseau JL, "Multiple myeloma: ESMO clinical recommendations for diagnosis, treatment and follow-up" 19 (19): 255-257, 2008

      11 Herman JG, "Methylationspecific PCR: a novel PCR assay for methylation status of CpG islands" 93 : 9821-9826, 1996

      12 Tanaka R, "Loss of function of p16 gene and prognosis of pulmonary adenocarcinoma" 103 : 608-615, 2005

      13 Hari PN, "Is the International Staging System superior to the Durie-Salmon staging system? A comparison in multiple myeloma patients undergoing autologous transplant" 23 : 1528-1534, 2009

      14 Durie BG, "International uniform response criteria for multiple myeloma" 20 : 1467-1473, 2006

      15 Greipp PR, "International staging system for multiple myeloma" 23 : 3412-3420, 2005

      16 Smadja NV, "Hypodiploidy is a major prognostic factor in multiple myeloma" 98 : 2229-2238, 2001

      17 Guzman LM, "High frequency of p16 promoter methylation in non-small cell lung carcinomas from Chile" 40 : 365-372, 2007

      18 Avet-Loiseau H, "Genetic abnormalities and survival in multiple myeloma: the experience of the Intergroupe Francophone du Myélome" 109 : 3489-3495, 2007

      19 Brenner H, "Expected long-term survival of patients diagnosed with multiple myeloma in 2006-2010" 94 : 270-275, 2009

      20 Yuregir OO, "Detecting methylation patterns of p16, MGMT, DAPK and E-cadherin genes in multiple myeloma patients" 32 : 142-149, 2010

      21 Zheng S, "Correlations of partial and extensive methylation at the p14(ARF) locus with reduced mRNA expression in colorectal cancer cell lines and clinicopathological features in primary tumors" 21 : 2057-2064, 2000

      22 Park G, "Concurrent p16 methylation pattern as an adverse prognostic factor in multiple myeloma: a methylation-specific polymerase chain reaction study using two different primer sets" SPRINGER 90/2011 (90/2011): 73-79, 2011

      23 Göhring G, "Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome" 116 : 3766-3769, 2010

      24 Jemal A, "Cancer statistics, 2008" 58 : 71-96, 2008

      25 Goto T, "Aberrant methylation of the p16 gene is frequently detected in advanced colorectal cancer" 29 : 275-277, 2009

      26 Martin P, "Aberrant gene promoter methylation in plasma cell dyscrasias" 84 : 256-261, 2008

      27 Durie BG, "A clinical staging system for multiple myeloma. Correlation of measured myeloma cell mass with presenting clinical features, response to treatment, and survival" 36 : 842-854, 1975

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2012-05-21 학술지명변경 한글명 : The Korean Journal of Laboratory Medicine -> Annals of Laboratory Medicine
      외국어명 : The Korean Journal of Laboratory Medicine -> Annals of Laboratory Medicine
      KCI등재
      2011-01-01 평가 학술지 분리 (기타) KCI등재
      2010-06-29 학술지명변경 한글명 : 대한진단검사의학회지 -> The Korean Journal of Laboratory Medicine KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.51 0.18 1.15
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.91 0.81 0.458 0.08
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