Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto Rico

被引:34
作者
De Jesus-Monge, Wilfredo E. [1 ,2 ,3 ]
Gonzalez-Keelan, Carmen [5 ]
Zhao, Ronghua [6 ,7 ]
Hamilton, Stanley R.
Rodriguez-Bigas, Miguel [8 ]
Cruz-Correa, Marcia [1 ,4 ,6 ,8 ,9 ]
机构
[1] Univ Puerto Rico, Dept Med, San Juan, PR 00936 USA
[2] Univ Massachusetts, Sch Med, Worcester, MA USA
[3] Univ Puerto Rico, Master Sci Clin Res Program, San Juan, PR 00936 USA
[4] Clin Res Ctr, San Juan, PR 00936 USA
[5] Univ Puerto Rico, Dept Pathol & Lab Med, San Juan, PR 00936 USA
[6] Univ Puerto Rico, Ctr Comprehens Canc, San Juan, PR 00936 USA
[7] Univ Saskatchewan, Coll Med, Dept Surg, Saskatoon, SK S7N 0W0, Canada
[8] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[9] Univ Puerto Rico, Dept Biochem, San Juan, PR 00936 USA
基金
美国国家卫生研究院;
关键词
Colorectal cancer; Genetics; Hispanics; Immunohistochemistry; Mismatch repair; TUMOR MICROSATELLITE-INSTABILITY; FAMILIAL ADENOMATOUS POLYPOSIS; REVISED BETHESDA GUIDELINES; NONPOLYPOSIS COLON-CANCER; LYNCH-SYNDROME; CLINICOPATHOLOGICAL FEATURES; ADJUVANT CHEMOTHERAPY; GERMLINE MUTATIONS; SERRATED POLYPS; DNA METHYLATION;
D O I
10.1007/s10689-009-9310-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) is a leading cause of morbidity and mortality and alterations in mismatch repair (MMR) genes, leading to absent protein (negative) expression, are responsible for approximately 20% of CRC cases. Immunohistochemistry is a tool for prescreening of MMR protein expression in CRC but the literature on its use on Hispanics is scarce. However, Hispanics represent the second leading ethnicity in the United States (US) and CRC is a public health burden in this group. Our objectives were to determine the frequency of MMR protein-negative CRC and to evaluate its association with clinical and pathological characteristics among Hispanics from Puerto Rico, for the first time to our knowledge. A retrospective observational study of unselected CRC patients from the Puerto Rico Medical Center from 2001 to 2005 was done. MLH1 and MSH2, the most commonly altered MMR genes, protein expression was evaluated using immunohistochemistry, with microsatellite instability (MSI) and BRAF gene analyses in the absence of MLH1 protein expression. One-hundred sixty-four CRC patients were evaluated: the overall MMR protein-negative frequency was 4.3%, with 0.6% frequency of co-occurrence of MLH1-protein negative expression, MSI-high, and normal BRAF gene. MMR protein-negative expression was associated with proximal colon location (P = 0.02) and poor histological tumor differentiation (P = 0.001), but not with other characteristics. The frequency of MMR protein-negative CRC in Hispanics from Puerto Rico was lower than reported in other populations. This finding may explain the lower CRC incidence rate among US Hispanics as compared to US non-Hispanic whites and blacks.
引用
收藏
页码:155 / 166
页数:12
相关论文
共 50 条
  • [21] Tumor and Patient Characteristics of Individuals with Mismatch Repair Deficient Colorectal Cancer
    Waldmann, Elisabeth
    Ferlitsch, Monika
    Binder, Nicolas
    Sellner, Franz
    Karner, Josef
    Heinisch, Birgit
    Klimpfinger, Martin
    Trauner, Michael
    DIGESTION, 2015, 91 (04) : 286 - 293
  • [22] Reduced expression of mismatch repair genes in colorectal cancer patients in Egypt
    Soliman, AS
    Bondy, ML
    Guan, Y
    El-Badawi, S
    Mokhtar, N
    Bayomi, S
    Raouf, AA
    Ismail, S
    McPherson, RS
    Abdel-Hakim, TF
    Beasley, RP
    Levin, B
    Wei, QY
    INTERNATIONAL JOURNAL OF ONCOLOGY, 1998, 12 (06) : 1315 - 1319
  • [23] Heterogenous mismatch-repair status in colorectal cancer
    Joost, Patrick
    Veurink, Nynke
    Holck, Susanne
    Klarskov, Louise
    Bojesen, Anders
    Harbo, Maria
    Baldetorp, Bo
    Rambech, Eva
    Nilbert, Mef
    DIAGNOSTIC PATHOLOGY, 2014, 9
  • [24] Immunohistochemistry staining for the mismatch repair proteins in the clinical care of patients with colorectal cancer
    South, Christopher D.
    Yearsley, Martha
    Martin, Edward
    Arnold, Mark
    Frankel, Wendy
    Hampel, Heather
    GENETICS IN MEDICINE, 2009, 11 (11) : 812 - 817
  • [25] Mismatch repair system in colorectal cancer. Frequency, cancer phenotype, and follow-up
    Rios-Valencia, J.
    Cruz-Reyes, C.
    Galindo-Garcia, T. A.
    Rosas-Camargo, V
    Gamboa-Dominguez, A.
    REVISTA DE GASTROENTEROLOGIA DE MEXICO, 2022, 87 (04): : 432 - 438
  • [26] Role of Deficient Mismatch Repair in the Personalized Management of Colorectal Cancer
    Zhang, Cong-Min
    Lv, Jin-Feng
    Gong, Liang
    Yu, Lin-Yu
    Chen, Xiao-Ping
    Zhou, Hong-Hao
    Fan, Lan
    INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2016, 13 (09)
  • [27] Mismatch repair polymorphisms and the risk of colorectal cancer
    Berndt, Sonja I.
    Platz, Elizabeth A.
    Fallin, M. Daniele
    Thuita, Lucy W.
    Hoffman, Sandra C.
    Helzlsouer, Kathy J.
    INTERNATIONAL JOURNAL OF CANCER, 2007, 120 (07) : 1548 - 1554
  • [28] Deficient Mismatch Repair and the Role of Immunotherapy in Metastatic Colorectal Cancer
    Quiroga, Dionisia
    Lyerly, H. Kim
    Morse, Michael A.
    CURRENT TREATMENT OPTIONS IN ONCOLOGY, 2016, 17 (08)
  • [29] MLH1 and MSH2 mismatch repair protein profile using immunohistochemistry in Nepalese colorectal cancer patients
    Bhattarai, Matrika
    Juhari, Wan Khairunnisa Wan
    Lama, Raju
    Pun, Chin Bahadur
    Yusof, Wardah
    Rahman, Wan Faiziah Wan Abdul
    Zakaria, Andee Dzulkarnaen
    Noordin, Khairul Bariah Ahmad Amin
    Shrestha, Tilak R.
    Zilfalil, Bin Alwi
    MEDICAL JOURNAL OF INDONESIA, 2020, 29 (02) : 183 - 189
  • [30] The current value of determining the mismatch repair status of colorectal cancer: A rationale for routine testing
    Ryan, E.
    Sheahan, K.
    Creavin, B.
    Mohan, H. M.
    Winter, D. C.
    CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2017, 116 : 38 - 57