The Applications of CRISPR/Cas9 System for Urinary System Tumor

被引:0
作者
Li, Shulin [1 ,2 ]
Wu, Yuqi [1 ,3 ]
Wang, Xiangwei [1 ,3 ]
机构
[1] Guangdong Med Univ, Dept Urol, Affiliated Hosp, Zhanjiang, Peoples R China
[2] Southern Univ Sci, Technol Hosp, Dept Urol, Shenzhen, Peoples R China
[3] Shenzhen Univ, Gen Hosp, Dept Urol, Shenzhen, Peoples R China
关键词
Urinary system tumor; CRISPR-Cas9; Gene editing; Gene therapy; Library screening; Genitourinary; BETA-GAMMA TRANSLOCATION; PROSTATE-CANCER; BLADDER-CANCER; RNA; DNA; RECEPTOR; REPEATS; PROTEIN; SCREEN; CELLS;
D O I
10.2174/1568026623666230504100706
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Tumors of the urinary system include those in the urinary and reproductive systems, of which tumors of the prostate, bladder, and kidney have the highest incidence. In recent years, due to changes in dietary structure, prostate cancer has become the most common type of male genitourinary system cancer. Furthermore, due to tobacco consumption, increases in industrialization, and the age of the population, the incidence of bladder cancer in both males and females in both urban and rural areas, has shown an increasing trend. The incidence and mortality of kidney cancer have also increased and negatively affected the lives and health of all residents. While surgery, radiotherapy, and chemotherapy have greatly improved the cure and survival rates of patients with urinary tumors, we lack methods for early detection and effective long-term treatment. New tools and methods for diagnosis and treatment are thus urgently needed. Recently, CRISPR/Cas9 has become an efficient method to alter the genome in many organisms. It can be used to activate or inhibit gene expression, which greatly facilitates the editing of targeted genes, both in vivo and in vitro. It provides a powerful scientific research tool to analyze the mechanisms of disease occurrence and development and to develop advanced targeted drug delivery. The diagnosis and treatment of human tumors will consequently be improved as this technology will surely accelerate cancer research. In this article, we discuss how CRISPR/Cas9 technology can be used to research and treat genitourinary system tumors will consequently be improved as this technology will surely accelerate cancer research. Here, we review the current applications of CRISPR/Cas9 technology for genitourinary system tumor research and therapy.
引用
收藏
页码:897 / 906
页数:10
相关论文
共 76 条
  • [1] FOXA1 knock-out via CRISPR/Cas9 altered Casp-9, Bax, CCND1, CDK4, and fibronectin expressions in LNCaP cells
    Albayrak, Gulsah
    Konac, Ece
    Dikmen, Asiye Ugras
    Bilen, Cenk Y.
    [J]. EXPERIMENTAL BIOLOGY AND MEDICINE, 2018, 243 (12) : 990 - 994
  • [2] Targeted nonviral gene therapy in prostate cancer
    Altwaijry, Najla
    Somani, Sukrut
    Dufes, Christine
    [J]. INTERNATIONAL JOURNAL OF NANOMEDICINE, 2018, 13 : 5753 - 5767
  • [3] Entering the Modern Era of Gene Therapy
    Anguela, Xavier M.
    High, Katherine A.
    [J]. ANNUAL REVIEW OF MEDICINE, VOL 70, 2019, 70 : 273 - 288
  • [4] CRISPR provides acquired resistance against viruses in prokaryotes
    Barrangou, Rodolphe
    Fremaux, Christophe
    Deveau, Helene
    Richards, Melissa
    Boyaval, Patrick
    Moineau, Sylvain
    Romero, Dennis A.
    Horvath, Philippe
    [J]. SCIENCE, 2007, 315 (5819) : 1709 - 1712
  • [5] CRISPR-Cas Systems: Prokaryotes Upgrade to Adaptive Immunity
    Barrangou, Rodolphe
    Marraffini, Luciano A.
    [J]. MOLECULAR CELL, 2014, 54 (02) : 234 - 244
  • [6] Evaluation of the CRISPR/Cas9 directed mutant TP53 gene repairing effect in human prostate cancer cell line PC-3
    Batir, Muhammet Burak
    Sahin, Ergin
    Cam, Fethi Sirri
    [J]. MOLECULAR BIOLOGY REPORTS, 2019, 46 (06) : 6471 - 6484
  • [7] Clustered regularly interspaced short palindrome repeats (CRISPRs) have spacers of extrachromosomal origin
    Bolotin, A
    Ouinquis, B
    Sorokin, A
    Ehrlich, SD
    [J]. MICROBIOLOGY-SGM, 2005, 151 : 2551 - 2561
  • [8] Significance of BRCA2 and RB1 Co-loss in Aggressive Prostate Cancer Progression
    Chakraborty, Goutam
    Armenia, Joshua
    Mazzu, Ying Z.
    Nandakumar, Subhiksha
    Stopsack, Konrad H.
    Atiq, Mohammad O.
    Komura, Kazumasa
    Jehane, Lina
    Hirani, Rahim
    Chadalavada, Kalyani
    Yoshikawa, Yuki
    Khan, Nabeela A.
    Chen, Yu
    Abida, Wassim
    Mucci, Lorelei A.
    Lee, Gwo-Shu Mary
    Nanjangud, Gouri J.
    Kantoff, Philip W.
    [J]. CLINICAL CANCER RESEARCH, 2020, 26 (08) : 2047 - 2064
  • [9] Dual Inhibition of PIK3C3 and FGFR as a New Therapeutic Approach to Treat Bladder Cancer
    Chen, Chun-Han
    Changou, Chun A.
    Hsieh, Tsung-Han
    Lee, Yu-Ching
    Chu, Cheng-Ying
    Hsu, Kai-Cheng
    Wang, Hao-Ching
    Lin, Yu-Chen
    Lo, Yan-Ni
    Liu, Yun-Ru
    Liou, Jing-Ping
    Yen, Yun
    [J]. CLINICAL CANCER RESEARCH, 2018, 24 (05) : 1176 - 1189
  • [10] Genome-wide CRISPR Screen in a Mouse Model of Tumor Growth and Metastasis
    Chen, Sidi
    Sanjana, Neville E.
    Zheng, Kaijie
    Shalem, Ophir
    Lee, Kyungheon
    Shi, Xi
    Scott, David A.
    Song, Jun
    Pan, Jen Q.
    Weissleder, Ralph
    Lee, Hakho
    Zhang, Feng
    Sharp, Phillip A.
    [J]. CELL, 2015, 160 (06) : 1246 - 1260