Seung Jo Kim
The Catholic University of America
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Featured researches published by Seung Jo Kim.
Journal of Surgical Oncology | 2009
Jin Hwi Kim; Joon Mo Lee; Ki Sung Ryu; Yong Seok Lee; Yong Gyu Park; Soo Young Hur; Keun Ho Lee; Sung Ha Lee; Seung Jo Kim
We evaluated the efficacy and feasibility of hyperthermic intraperitoneal chemotherapy (HIPEC) using paclitaxel as consolidation therapy in patients with epithelial ovarian cancer.
Cancer Letters | 1999
Jong Sup Park; Seung Myung Dong; Hy Sook Kim; Jung Young Lee; Soo-Jong Um; In Seo Park; Seung Jo Kim; Sung Eun Namkoong
The p16 gene was identified as cyclin-dependent kinase inhibitor (CDKI) and this may negatively regulate the cell cycle by acting as a tumor suppressor. Using tissue microdissection, the molecular changes at p16 and Rb genes were analysed in the spectrum of disease from dysplasia to invasive cancer of the uterine cervix. Six of 27 (22%) cases informative for D9S171 and IFNA of 9p21-22 marker (p16INK4a) showed loss of one or both alleles in at least one of these loci. LOH of pRb was detected in 29% (5/17). Gene alterations at p16 and pRb loci were only detectable in some cases of HPV-16/18 DNA positive cervical cancer. Three cases demonstrated mutational changes of p16INK4a, and the alterations were determined to be G to T shift, suggesting transitional missense mutation. In summary, the inactivation of the p16/cdk-cyclin/Rb cascade may play an additional role during the malignant progression in HPV-16/18 positive cervical cancers.
Gynecologic Oncology | 1991
Jong Sup Park; Sung Eun Namkoong; Hun Young Lee; Seung Jo Kim; Richard W. Daniel; Keerti V. Shah
The histopathologic features of cervical dysplasia (20 cases) and cervical carcinoma (15 cases) in Korean women were correlated with the presence of human papillomaviruses (HPVs) as determined by polymerase chain reaction technology on paraffin-processed specimens. A segment of the E6 open reading frame of several HPV types (HPV 6, 11, 16, 18, 31, 33, and 35) was amplified using primers which were synthesized to contain 50% G + C, in order to give optimum annealing for the amplification of HPVs. All specimens were also tested for amplification of the cellular beta-globin gene. HPV was found in 19 (54%) cases. The HPV types were HPV 6 in 1 case (3%), HPV 16 in 15 cases (43%), HPV 18 in 2 cases (6%), and HPV 33 in 3 cases (9%). HPV was identified in 16 of 25 (64%) beta-globin-positive and 3 of 10 (30%) beta-globin-negative tissues. HPV types 11, 31, and 35 were not detected in any of the specimens. HPV 6, 18, and 33 were detected only in preneoplastic lesions, and co-infection with these three viruses was observed in one case of severe dysplasia. HPV type 16 was found in 8 (40%) premalignant lesions and in 7 (47%) invasive carcinomas. These data indicate that HPVs are found along the entire spectrum of cervical neoplasia. HPV 16 was the predominant virus in invasive cancer of the cervix.
Gynecologic Oncology | 1995
Sung Eun Namkoong; Jong Sup Park; Jin Woo Kim; Seog Nyeon Bae; Gu Taek Han; Joon Mo Lee; Jae Keun Jung; Seung Jo Kim
Gynecologic Oncology | 1998
Seung Jo Kim; Seog Nyeon Bae; Jae Hoon Kim; Chan Joo Kim; Jae Keun Jung
Gynecologic Oncology | 1998
Jong Sup Park; Dong Choon Park; Chan Joo Kim; Hee Kyung Ahn; Soo-Jong Um; Sue Nie Park; Seung Jo Kim; Sung Eun Namkoong
Gynecologic Oncology | 1997
Seog Nyeon Bae; Sung Eun Namkoong; Jae Keun Jung; Chan Joo Kim; Jong Sup Park; Jin Woo Kim; Joon Mo Lee; Seung Jo Kim
Gynecologic Oncology | 1996
Jong Sup Park; Ki Sung Rhyu; Chan Joo Kim; Hy Sook Kim; Ku Taek Han; Hee Kyoung Ahn; Seung Jo Kim; Sung Eun Namkoong
Gynecologic Oncology | 1995
Yong Hun Chee; Sung Eun Namkoong; Dae Hoon Kim; Seung Jo Kim; Jong Sup Park
Gynecologic Oncology | 1994
Jong Sup Park; Yong Hun Chee; Sung Eun Namkoong; Sang Kyun Han; Tae Eung Kim; Hun Young Lee; Seung Jo Kim