Differential expression of microRNA between triple negative breast cancer patients of African American and European American descent

被引:5
|
作者
MacCuaig, William M. [1 ,2 ]
Thomas, Alexandra [3 ]
Claros-Sorto, Juan C. [1 ,4 ]
Gomez-Gutierrez, Jorge G. [5 ]
Alexander, Adam C. [1 ,6 ]
Wellberg, Elizabeth A. [1 ,7 ]
Grizzle, William E. [8 ]
McNally, Lacey R. [1 ,4 ]
机构
[1] Univ Oklahoma, Stephenson Canc Ctr, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Dept Biomed Engn, Norman, OK USA
[3] Wake Forest Baptist Hlth, Dept Hematol Oncol, Winston Salem, NC USA
[4] Univ Oklahoma, Dept Surg, Oklahoma City, OK 73104 USA
[5] Univ Missouri, Dept Child Hlth, Columbia, MO 65201 USA
[6] Univ Oklahoma, Dept Family & Prevent Med, Oklahoma City, OK 73104 USA
[7] Univ Oklahoma, Dept Pathol, Oklahoma City, OK 73104 USA
[8] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
关键词
African American; European American; Caucasian; human; laser-capture microdissection; microRNA; racial disparity; triple negative breast cancer; HEPATOCELLULAR-CARCINOMA CELL; PROSTATE-CANCER; ADIPOSE-TISSUE; PROLIFERATION; INFLAMMATION; INVASION; MICROENVIRONMENT; RADIORESISTANCE; METASTASIS; RESISTANCE;
D O I
10.1080/10520295.2021.2005147
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
There are racial disparities in the outcome of triple negative breast cancer (TNBC) patients between women of African ancestry and women of European ancestry, even after accounting for lifestyle, socioeconomic and clinical factors. MicroRNA (miRNA) are non-coding molecules whose level of expression is associated with cancer suppression, proliferation and drug resistance; therefore, these have potential for biomarker applications in cancers including TNBC. Historically, miRNAs up-regulated in African American (AA) patients have received less attention than for patients of European ancestry. Using laser capture microdissection (LCM) to acquire ultrapure tumor cell samples, miRNA expression was evaluated in 15 AA and 15 European American (EA) TNBC patients. Tumor sections were evaluated using RNA extraction followed by miRNA analysis and profiling. Results were compared based on ethnicity and method of tissue fixation. miRNAs that showed high differential expression in AA TNBC patients compared to EA included: miR-19a, miR-192, miR-302a, miR-302b, miR-302c, miR-335, miR-520b, miR-520f and miR-645. LCM is a useful technique for isolation of tumor cells. We found a greater abundance of RNA in frozen samples compared to formalin fixed, paraffin embedded samples. miRNA appears to be a useful biomarker for TNBC to improve diagnosis and treatment.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 50 条
  • [21] Microbiome diversity in African American, European American, and Egyptian colorectal cancer patients
    Elkholy, Amr
    Avuthu, Nagavardhini
    Abdalla, Mohammed
    Behring, Michael
    Bajpai, Prachi
    Kim, Hyung-Gyoon
    Header, Doaa
    Elwafa, Reham AH. Abo
    Saed, Hesham
    Embaby, Amira
    El-Nikhely, Nefertiti
    Obuya, Sarah
    Mohamed, Mostafa
    Badawy, Ahmed Ashour
    Nawar, Ahmed
    Afaq, Farrukh
    Rogers, Laura Q.
    Bae, Sejong
    Shikany, James M.
    Bateman, Lori Brand
    Fouad, Mona
    Saleh, Mansoor
    Samuel, Temesgen
    Varambally, Sooryanarayana
    Guda, Chittibabu
    Arafat, Waleed
    Manne, Upender
    HELIYON, 2023, 9 (07)
  • [22] Differences in microRNA expression in breast cancer between women of African and European ancestry
    Gong, Zhihong
    Wang, Jie
    Wang, Dan
    Buas, Matthew F.
    Ren, Xuefeng
    Freudenheim, Jo L.
    Belinsky, Steven A.
    Liu, Song
    Ambrosone, Christine B.
    Higgins, Michael J.
    CARCINOGENESIS, 2019, 40 (01) : 61 - 69
  • [23] Prognostic value of microRNA-9 and microRNA-155 expression in triple-negative breast cancer
    Jang, Min Hye
    Kim, Hyun Jeong
    Gwak, Jae Moon
    Chung, Yul Ri
    Park, So Yeon
    HUMAN PATHOLOGY, 2017, 68 : 69 - 78
  • [24] Immune microenvironment of triple-negative breast cancer in African-American and Caucasian women
    Tess O’Meara
    Anton Safonov
    David Casadevall
    Tao Qing
    Andrea Silber
    Brigid Killelea
    Christos Hatzis
    Lajos Pusztai
    Breast Cancer Research and Treatment, 2019, 175 : 247 - 259
  • [25] Biopsychosocial Challenges and Needs of Young African American Women with Triple-Negative Breast Cancer
    Bollinger, Sarah
    HEALTH & SOCIAL WORK, 2018, 43 (02) : 84 - 92
  • [26] Immune microenvironment of triple-negative breast cancer in African-American and Caucasian women
    O'Meara, Tess
    Safonov, Anton
    Casadevall, David
    Qing, Tao
    Silber, Andrea
    Killelea, Brigid
    Hatzis, Christos
    Pusztai, Lajos
    BREAST CANCER RESEARCH AND TREATMENT, 2019, 175 (01) : 247 - 259
  • [27] Identification of novel biomarkers differentially expressed between African-American and Caucasian-American prostate cancer patients
    Ye, Fei
    Han, Xiaoxia
    Shao, Yonzhao
    Lo, Jingzhi
    Zhang, Fengxia
    Wang, Jinhua
    Melamed, Jonathan
    Deng, Fang-Ming
    Sfanos, Karen S.
    De Marzo, Angelo
    Ren, Guoping
    Wang, Dongwen
    Zhang, David
    Lee, Peng
    AMERICAN JOURNAL OF CANCER RESEARCH, 2022, 12 (04): : 1660 - +
  • [28] Glucocorticoid receptor overexpression slightly shifts microRNA expression patterns in triple-negative breast cancer
    Buschman, Dominik
    Gonzalez, Ricardo
    Kirchner, Benedikt
    Mazzone, Claudia
    Pfaffl, Michael W.
    Schelling, Gustav
    Steinlein, Ortrud
    Reithmair, Marlene
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2018, 52 (06) : 1765 - 1776
  • [29] Commentary: Genomic, epigenomic, and transcriptomic signatures of prostate cancer between African American and European American patients
    Rollin, Francois G.
    Krishnamurthy, Sudarshan
    Beriwal, Surabhi
    FRONTIERS IN ONCOLOGY, 2023, 13
  • [30] Hsa_circ_0091074 regulates TAZ expression via microRNA-1297 in triple negative breast cancer cells
    Hu, Jiashu
    Ji, Changle
    Hua, Kaiyao
    Wang, Xuehui
    Deng, Xiaochong
    Li, Jiayi
    Graham, Dinny
    Fang, Lin
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2020, 56 (05) : 1314 - 1326