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Kyung Mi Kim

Sungkyunkwan University · Medicine

About the Lab

Professor Kyung Mi Kim's research lab specializes in gastrointestinal oncology and molecular pathology, with a focus on the genetic and molecular mechanisms underlying gastric cancer and colorectal neoplasms. The lab investigates novel biomarkers such as SLC34A2-ROS1 rearrangements and tumor mutational burden (TMB) to guide targeted and immunotherapeutic strategies in advanced gastric cancer. It also explores the pathogenesis and molecular profiles of serrated polyps, including sessile serrated adenomas and traditional serrated adenomas, with particular attention to ethnic and geographic variations in disease presentation. The lab integrates clinical, pathological, and genomic data to improve early detection and personalized treatment approaches for gastrointestinal malignancies.

gastric cancertumor mutational burdenserrated polypsmolecular oncologytargeted therapy

Research Overview

Papers
453
Total Citations
20,048
Papers (5y)
57
Primary Field
Medicine

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
57total
2022
2023
2024
2025
2026
Citations per year (5y)
622total
20222023202420252026

Selected Papers

15
1
Article|154 citations·2014
Deregulation of Immune Response Genes in Patients With Epstein-Barr Virus-Associated Gastric Cancer and Outcomes
Sun Young Kim, Charny Park, Ha‐Jung Kim, Jihyun Park, Jinha Hwang, Jong‐Il Kim, Min Gew Choi, Sung Hoon Kim, Kyoung‐Mee Kim, Myung-Soo Kang
SJR Q1Gastroenterology
OncologyMedicine
2
Article|133 citations·2011
Molecular Features of Colorectal Hyperplastic Polyps and Sessile Serrated Adenoma/Polyps From Korea
Kyoung‐Mee Kim, Eui Jin Lee, Sang‐Yun Ha, So Young Kang, Kee‐Taek Jang, Cheol Keun Park, Jin Yong Kim, Young Ho Kim, Dong Kyung Chang, Robert D. Odze
SJR Q1The American Journal of Surgical Pathology

Abundant recent data suggest that sessile serrated adenoma/polyp (SSA/P) is an early precursor lesion in the serrated pathway of carcinogenesis. It is believed that SSA/Ps develop cancer by an SSA/P-dysplasia-carcinoma sequence. Hyperplastic polyps (HPs) share some histologic and molecular characteristics with SSA/P, but it is unclear whether SSA/Ps are derived from HPs or whether they develop by a different pathogenetic pathway. Previous studies have shown that serrated polyps from Korean patie

OncologyMedicine
3
Article|123 citations·2013
MET overexpression assessed by new interpretation method predicts gene amplification and poor survival in advanced gastric carcinomas
Sang Yun Ha, Jeeyun Lee, So Young Kang, In‐Gu Do, Soomin Ahn, Joon Oh Park, Won Ki Kang, Min-Gew Choi, Tae Sung Sohn, Jae Moon Bae, Sung Kim, Min‐Ji Kim
SJR Q1Modern PathologyOA
SurgeryMedicine
4
Article|122 citations·2004
Progressive methylation during the serrated neoplasia pathway of the colorectum
Seung Myung Dong, Eui J Lee, Eun Sook Jeon, Cheol K. Park, Kyoung‐Mee Kim
SJR Q1Modern PathologyOA
Pathology and Forensic MedicineMedicine
5
Article|120 citations·2013
Identification of ROS1 rearrangement in gastric adenocarcinoma
Jeeyun Lee, Seung Eun Lee, So Young Kang, In‐Gu Do, Sujin Lee, Sang Yun Ha, Jeonghee Cho, Won Ki Kang, Jiryeon Jang, Sai‐Hong Ignatius Ou, Kyoung‐Mee Kim
SJR Q1Cancer

BACKGROUND: Recently, chromosomal rearrangements involving receptor tyrosine kinases (RTKs) have been described in common epithelial malignancies, including nonsmall cell lung cancer (NSCLC), colorectal cancer, and breast cancer. One of these RTKs, c-ros oncogene 1, receptor tyrosine kinase (ROS1), has been identified as a driver mutation in NSCLC, because its inhibition by crizotinib, an anaplastic lymphoma receptor tyrosine kinase (ALK)/met proto-oncogene hepatocyte growth factor receptor (MET

OncologyMedicine
6
Article|110 citations·2016
FGFR2 in gastric cancer: protein overexpression predicts gene amplification and high H-index predicts poor survival
Soomin Ahn, Jeeyun Lee, Min Eui Hong, Seung Tae Kim, Se Hoon Park, Min Gew Choi, Junho Lee, Tae Sung Sohn, Jae Moon Bae, Sung Kim, Sin‐Ho Jung, Won Ki Kang
SJR Q1Modern PathologyOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology
7
Review|108 citations·2002
Methylation reveals a niche: stem cell succession in human colon crypts
Kyoung‐Mee Kim, Darryl Shibata
SJR Q1Oncogene
Pathology and Forensic MedicineMedicine
8
Article|106 citations·2010
KRAS Mutations in Traditional Serrated Adenomas From Korea Herald an Aggressive Phenotype
Kyoung‐Mee Kim, Eui Jin Lee, Youngho Kim, Dong Kyung Chang, Robert D. Odze
SJR Q1The American Journal of Surgical Pathology

The pathogenesis and risk of malignancy of traditional serrated adenomas (TSAs) are unclear. In North America, TSAs are relatively uncommon, occur mainly in the left colon, and in some studies, have not been shown to have a strong association with hyperplastic polyp (HPP) or sessile polyp adenoma (SSA) precursor lesions. In the Far East, and particularly in Korea, TSAs are more common and occur both in the left and right colon. However, the pathogenesis of TSAs in Korean patients, and the simila

Pathology and Forensic MedicineMedicine
9
Article|100 citations·2005
Gastrointestinal Stromal Tumors in Koreans: It's Incidence and the Clinical, Pathologic and Immunohistochemical Findings
Kyoung‐Mee Kim, Dong‐Wook Kang, Woo Sung Moon, Jae Bok Park, Cheol Keun Park, Jin Hee Sohn, Jin Sook Jeong, Mee-Yon Cho, So‐Young Jin, Jong Sang Choi, Dae Young Kang, The Korean Gastrointestinal Pathology Study Group
SJR Q2Journal of Korean Medical ScienceOA

Seven hundred forty seven cases of gastrointestinal stromal tumors (GISTs) in Koreans who were diagnosed between 2001 and 2002 were analyzed to evaluate their occurrence and their clinical, pathologic and immunohistochemical findings. The most frequent location of tumor was in the stomach (63%), followed by the small intestine (30%), the colorectum (5%), and the esophagus (2%). c-kit expression was found in 93.6% of the cases, while CD34, SMA and S-100 protein was positive in 80.1%, 28.2%, and 2

GastroenterologyMedicine
10
Article|94 citations·2020
Tumor Mutational Burden Determined by Panel Sequencing Predicts Survival After Immunotherapy in Patients With Advanced Gastric Cancer
Jinchul Kim, Binnari Kim, So Young Kang, You Jeong Heo, Se Hoon Park, Seung Tae Kim, Won Ki Kang, Jeeyun Lee, Kyoung‐Mee Kim
SJR Q2Frontiers in OncologyOA

<b>Objective:</b> Panel-based sequencing is widely used to measure tumor mutational burden (TMB) in clinical trials and is ready to enter routine diagnostics. However, cut-off points to distinguish "TMB-high" from "TMB-low" tumors are not consistent and the clinical implications of TMB in predicting responses to immune checkpoint blockade (ICB) in gastric cancer are not clearly defined. We aimed to assess whether TMB is associated with the response to immunotherapy and to examine its relation wi

GastroenterologyMedicine
11
Article|94 citations·2021
PD-L1 expression in gastric cancer: interchangeability of 22C3 and 28-8 pharmDx assays for responses to immunotherapy
Soomin Ahn, Kyoung‐Mee Kim
SJR Q1Modern PathologyOA
OncologyMedicine
12
Article|93 citations·2004
Granulomatous Gastritis
Lee-So Maeng, Anhi Lee, Kyu-Yong Choi, Chang Suk Kang, Kyoung‐Mee Kim
SJR Q1The American Journal of Surgical Pathology

Granulomas in gastric biopsy specimens are extremely rare, and in Western countries, more than half are associated with Crohn's disease. To evaluate the incidence and their etiology in a gastric carcinoma (and Helicobater pylori infection)-prevalent area, gastric mucosal biopsies were reviewed and their clinicopathologic findings were analyzed. The clinicopathologic diagnoses of the 18 patients with granulomatous gastritis were as follows: chronic gastritis with (n = 14) and without (n = 1) H. p

SurgeryMedicine
13
Article|87 citations·2001
Genetic evidence for the multi-step progression of mixed glandular–neuroendocrine gastric carcinomas
Kyoung‐Mee Kim, Minjoo Kim, Bo-Kyoung Cho, Sang‐Wook Choi, Mun‐Gan Rhyu
SJR Q1Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin
EpidemiologyMedicine
14
Article|81 citations·2018
Four distinct immune microenvironment subtypes in gastric adenocarcinoma with special reference to microsatellite instability
Junhun Cho, Young Hwan Chang, You Jeong Heo, SeungTae Kim, Nayoung K. D. Kim, Joon Oh Park, Won Ki Kang, Jeeyun Lee, Kyoung‐Mee Kim
SJR Q1ESMO OpenOA

GC can be classified into four TME types based on PD-L1 and TIL, and numbers of frameshift mutation correlate well with PD-L1 expression in MSI-H GC.

OncologyMedicine
15
Article|80 citations·2011
The CpG island methylator phenotype may confer a survival benefit in patients with stage II or III colorectal carcinomas receiving fluoropyrimidine-based adjuvant chemotherapy
Byung‐Hoon Min, Jeong Mo Bae, Eui Jin Lee, Hong Yu, Young‐Ho Kim, Dong Kyung Chang, Hee Cheol Kim, Cheol Keun Park, Suk‐Hee Lee, Kyoung‐Mee Kim, Gyeong Hoon Kang
SJR Q2BMC CancerOA

BACKGROUND: Colorectal carcinoma (CRC) with CpG island methylator phenotype (CIMP) is recognized as a distinct subgroup of CRC, and CIMP status affects prognosis and response to chemotherapy. Identification of CIMP status in CRC is important for proper patient management. In Eastern countries, however, the clinicopathologic and molecular characteristics and prognosis of CRCs with CIMP are still unclear. METHODS: A total of 245 patients who underwent their first surgical resection for sporadic CR

Molecular BiologyBiochemistry, Genetics and Molecular Biology

Research Areas

Pulmonary and Respiratory MedicineOncologyMolecular BiologyPathology and Forensic MedicineGastroenterologyCancer Research

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