Abstract
A novel gene editing tool, the Cas system, associated with the CRISPR system, is emerging as a potential method for genome modification. This simple method, based on the adaptive immune defense system of prokaryotes, has been developed and used in human cancer research. These technologies have tremendous therapeutic potential, especially in gene therapy, where a patient-specific mutation is genetically corrected to cure diseases that cannot be cured with conventional treatments. However, translating CRISPR/Cas9 into the clinic will be challenging, as we still need to improve the efficiency, specificity, and application of the technology. In this review, we will explain how CRISPR-Cas9 technology can treat cancer at the molecular level, focusing on ordination and the epigenome. We will also focus on the promise and shortcomings of this system to ensure its application in the treatment and prevention of cancer.
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References
Abudayyeh OO, Gootenberg JS, Konermann S, Joung J, Slaymaker IM, Cox DB et al (2016) C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector. Science 353:6299
Alves E, Taifour S, Dolcetti R, Chee J, Nowak AK, Gaudieri S, Blancafort P (2021) Reprogramming the anti-tumor immune response via CRISPR genetic and epigenetic editing. Mol Ther Methods Clin Dev. https://doi.org/10.1016/j.omtm.2021.04.009
Anand P, Kunnumakara AB, Sundaram C, Harikumar KB, Tharakan ST, Lai OS et al (2008) Cancer is a preventable disease that requires major lifestyle changes. Pharm Res 25(9):2097–2116
Arechavaleta-Velasco F, Perez-Juarez CE, Gerton GL, Diaz-Cueto L (2017) Progranulin and its biological effects in cancer. Med Oncol 34(12):1–11
Asad AS, Moreno Ayala MA, Gottardo MF, Zuccato C, Nicola Candia AJ, Zanetti FA et al (2017) Viral gene therapy for breast cancer: progress and challenges. Expert Opin Biol Ther 17(8):945–959
Bakondi B, Lv W, Lu B, Jones MK, Tsai Y, Kim KJ et al (2016) In vivo CRISPR/Cas9 gene editing corrects retinal dystrophy in the S334ter-3 rat model of autosomal dominant retinitis pigmentosa. Mol Ther 24(3):556–563
Barrangou R, Fremaux C, Deveau H, Richards M, Boyaval P, Moineau S et al (2007) CRISPR provides acquired resistance against viruses in prokaryotes. Science 315(5819):1709–1712
Beltran AS, Blancafort P (2011) Reactivation of MASPIN in non-small cell lung carcinoma (NSCLC) cells by artificial transcription factors (ATFs). Epigenetics 6(2):224–235
Benamar M, Guessous F, Du K, Corbett P, Obeid J, Gioeli D et al (2016) Inactivation of the CRL4-CDT2-SET8/p21 ubiquitylation and degradation axis underlies the therapeutic efficacy of pevonedistat in melanoma. EBioMedicine 10:85–100
Berardi R, Torniai M, Lenci E, Pecci F, Morgese F, Rinaldi S (2019) Electrolyte disorders in cancer patients: a systematic review. J Cancer Metast Treat. https://doi.org/10.20517/2394-4722.2019.008
Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A (2018) Global cancer statistics 2018 GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA 68(6):394–424
Brown A, Winter J, Gapinske M, Tague N, Woods WS, Perez-Pinera P (2019) Multiplexed and tunable transcriptional activation by promoter insertion using nuclease-assisted vector integration. Nucleic Acids Res 47:e67
Brunet E, Jasin M (2018) Induction of chromosomal translocations with CRISPR-Cas9 and other nucleases: understanding the repair mechanisms that give rise to translocations. In: Zhang Y (ed) Chromosome translocation. Springer, Singapore, pp 15–25
Bu X, Kato J, Hong JA, Merino MJ, Schrump DS, Lund FE, Moss J (2018) CD38 knockout suppresses tumorigenesis in mice and clonogenic growth of human lung cancer cells. Carcinogenesis 39(2):242–251
Burmistrz M, Krakowski K, Krawczyk-Balska A (2020) RNA-targeting CRISPR–Cas systems and their applications. Int J Mol Sci 21(3):1122
Campa CC, Weisbach NR, Santinha AJ, Incarnato D, Platt RJ (2019) Multiplexed genome engineering by Cas12a and CRISPR arrays encoded on single transcripts. Nat Methods 16:887–893
Chen C, Liu Y, Rappaport AR, Kitzing T, Schultz N, Zhao Z et al (2014a) MLL3 is a haploinsufficient 7q tumor suppressor in acute myeloid leukemia. Cancer Cell 25(5):652–665
Chen H, Choi J, Bailey S (2014b) Cut site selection by the two nuclease domains of the Cas9 RNA-guided endonuclease. J Biol Chem 289(19):13284–13294
Chen B, Liu J, Ho TT, Ding X, Mo YY (2016) ERK-mediated NF-κB activation through ASIC1 in response to acidosis. Oncogenesis 5(12):e279–e279
Chen JS, Ma E, Harrington LB, Da Costa M, Tian X, Palefsky JM, Doudna JA (2018) CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity. Science 360(6387):436–439
Chen M, Mao A, Xu M, Weng Q, Mao J, Ji J (2019) CRISPR-Cas9 for cancer therapy: opportunities and challenges. Cancer Lett 447:48–55
Chira S, Gulei D, Hajitou A, Berindan-Neagoe I (2018) Restoring the p53 ‘Guardian’phenotype in p53-deficient tumor cells with CRISPR/Cas9. Trends Biotechnol 36(7):653–660
Cho SW, Kim S, Kim Y, Kweon J, Kim HS, Bae S, Kim JS (2014) Analysis of off-target effects of CRISPR/Cas-derived RNA-guided endonucleases and nickases. Genome Res 24(1):132–141
Choi PS, Meyerson M (2014) Targeted genomic rearrangements using CRISPR/Cas technology. Nat Commun 5(1):1–6
Chylinski K, Le Rhun A, Charpentier E (2013) The tracrRNA and Cas9 families of type II CRISPR-Cas immunity systems. RNA Biol 10(5):726–737
Cong L, Ran FA, Cox D, Lin S, Barretto R, Habib N et al (2013) Multiplex genome engineering using CRISPR/Cas systems. Science 339(6121):819–823
Costa JR, Bejcek BE, McGee JE, Fogel AI, Brimacombe KR, Ketteler R (2017) Genome editing using engineered nucleases and their use in genomic screening. In Assay Guidance Manual [Internet]. Eli Lilly & Company and the National Center for Advancing Translational Sciences
Ding Q, Regan SN, Xia Y, Oostrom LA, Cowan CA, Musunuru K (2013) Enhanced efficiency of human pluripotent stem cell genome editing through replacing TALENs with CRISPRs. Cell Stem Cell 12(4):393
Dyda F, Hickman AB (2015) Mechanism of spacer integration links the CRISPR/Cas system to transposition as a form of mobile DNA. Mob DNA 6(1):1–5
Fellmann C, Gowen BG, Lin PC, Doudna JA, Corn JE (2017) Cornerstones of CRISPR–Cas in drug discovery and therapy. Nat Rev Drug Discov 16(2):89–100
Fidler MM, Bray F (2018) Global cancer inequalities. Front Oncol 8:293
Fujii M, Clevers H, Sato T (2019) Modeling human digestive diseases with CRISPR-Cas9–modified organoids. Gastroenterology 156(3):562–576
Gaj T, Epstein BE, Schaffer DV (2016) Genome engineering using adeno-associated virus: basic and clinical research applications. Mol Ther 24(3):458–464
Ghezraoui H, Piganeau M, Renouf B, Renaud JB, Sallmyr A, Ruis B et al (2014) Chromosomal translocations in human cells are generated by canonical nonhomologous end-joining. Mol Cell 55(6):829–842
Gootenberg JS, Abudayyeh OO, Lee JW, Essletzbichler P, Dy AJ, Joung J et al (2017) Nucleic acid detection with CRISPR-Cas13a/C2c2. Science 356(6336):438–442
Gunel NS, Birden N, Kurt CC, Bagca BG, Shademan B, Sogutlu F, Ozates NP, Avci CB (2021) Effect of valproic acid on miRNAs affecting histone deacetylase in a model of anaplastic thyroid cancer. Mol Biol Rep 48:6085–6091
Gupta RM, Musunuru K (2014) Expanding the genetic editing tool kit: ZFNs, TALENs, and CRISPR-Cas9. J Clin Investig 124(10):4154–4161
Haapaniemi E, Botla S, Persson J, Schmierer B, Taipale J (2018) CRISPR–Cas9 genome editing induces a p53-mediated DNA damage response. Nat Med 24(7):927–930
Han HA, Pang JKS, Soh BS (2020) Mitigating off-target effects in CRISPR/Cas9-mediated in vivo gene editing. J Mol Med 98(5):615–632
Harrod A, Fulton J, Nguyen VT, Periyasamy M, Ramos-Garcia L, Lai CF et al (2017) Genomic modelling of the ESR1 Y537S mutation for evaluating function and new therapeutic approaches for metastatic breast cancer. Oncogene 36(16):2286–2296
Hart T, Chandrashekhar M, Aregger M, Steinhart Z, Brown KR, MacLeod G et al (2015) High-resolution CRISPR screens reveal fitness genes and genotype-specific cancer liabilities. Cell 163(6):1515–1526
He H, Liu X, Liu Y, Zhang M, Lai Y, Hao Y, Wang Q, Shi D, Wang N, Luo XG, Ma W (2019) Human papillomavirus E6/E7 and long noncoding RNA TMPOP2 mutually upregulated gene expression in cervical cancer cells. J Virol 93(8):e01808-e1818
Hofacker D, Broche J, Laistner L, Adam S, Bashtrykov P, Jeltsch A (2020) Engineering of effector domains for targeted DNA methylation with reduced offtarget effects. Int J Mol Sci 21:502
Hu Z, Yu L, Zhu D, Ding W, Wang X, Zhang C, Wang L, Jiang X, Shen H, He D, Li K (2014) Disruption of HPV16-E7 by CRISPR/Cas system induces apoptosis and growth inhibition in HPV16 positive human cervical cancer cells. BioMed Res Int. https://doi.org/10.1155/2014/612823
Huang Y-H, Su J, Lei Y, Brunetti L, Gundry MC, Zhang X, Jeong M, Li W, Goodell MA (2017) DNA epigenome editing using CRISPR-Cas SunTagdirected DNMT3A. Genome Biol 18:176
Ihry RJ, Worringer KA, Salick MR, Frias E, Ho D, Theriault K et al (2018) p53 inhibits CRISPR–Cas9 engineering in human pluripotent stem cells. Nat Med 24(7):939–946
Isazadeh A, Hajazimian S, Shadman B, Safaei S, Bedoustani AB, Chavoshi R et al (2020) Anti-cancer effects of probiotic Lactobacillus acidophilus for colorectal cancer cell line caco-2 through apoptosis induction. Pharmaceutical Sciences 27(2):262–267
Jadid MFS, Shademan B, Chavoshi R, Seyyedsani N, Aghaei E, Taheri E et al (2021) Enhanced anticancer potency of hydroxytyrosol and curcumin by PLGA-PAA nano-encapsulation on PANC-1 pancreatic cancer cell line. Environ Toxicol 36(6):1043–1051
Jansen R, Embden JDV, Gaastra W, Schouls LM (2002a) Identification of genes that are associated with DNA repeats in prokaryotes. Mol Microbiol 43(6):1565–1575
Jansen R, van Embden JD, Gaastra W, Schouls LM (2002b) Identification of a novel family of sequence repeats among prokaryotes. OMICS 6(1):23–33
Jiang F, Doudna JA (2017) CRISPR–Cas9 structures and mechanisms. Annu Rev Biophys 46:505–529
Jinek M, Chylinski K, Fonfara I, Hauer M, Doudna JA, Charpentier E (2012) A programmable dual-RNA–guided DNA endonuclease in adaptive bacterial immunity. Science 337(6096):816–821
Khalaf K, Janowicz K, Dyszkiewicz-Konwińska M, Hutchings G, Dompe C, Moncrieff L et al (2020) CRISPR/Cas9 in cancer immunotherapy: animal models and human clinical trials. Genes 11(8):921
Kim S, Kim D, Cho SW, Kim J, Kim JS (2014) Highly efficient RNA-guided genome editing in human cells via delivery of purified Cas9 ribonucleoproteins. Genome Res 24(6):1012–1019
Kline CLB, Ralff MD, Lulla AR, Wagner JM, Abbosh PH, Dicker DT et al (2018) Role of dopamine receptors in the anticancer activity of ONC201. Neoplasia 20(1):80–91
Koike-Yusa H, Li Y, Tan EP, Velasco-Herrera MDC, Yusa K (2014) Genome-wide recessive genetic screening in mammalian cells with a lentiviral CRISPR-guide RNA library. Nat Biotechnol 32(3):267–273
Lai J, Wang H, Luo Q, Huang S, Lin S, Zheng Y, Chen Q (2017) The relationship between DNA methylation and Reprimo gene expression in gastric cancer cells. Oncotarget 8(65):108610
Lertsuwan K, Choe LH, Marwa IR, Lee K, Sikes RA (2017) Identification of fibulin-1 as a human bone marrow stromal (HS-5) cell-derived factor that induces human prostate cancer cell death. Prostate 77(7):729–742
Leung THY, Tang HWM, Siu MKY, Chan DW, Chan KKL, Cheung ANY, Ngan HYS (2018) Human papillomavirus E6 protein enriches the CD55 (+) population in cervical cancer cells, promoting radioresistance and cancer aggressiveness. J Pathol 244(2):151–163
Li H, Yang Y, Hong W, Huang M, Wu M, Zhao X (2020) Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects. Signal Transduct Target Ther 5(1):1–23
Lino CA, Harper JC, Carney JP, Timlin JA (2018) Delivering CRISPR: a review of the challenges and approaches. Drug Deliv 25(1):1234–1257
Liu Y, Tao W, Wen S, Li Z, Yang A, Deng Z, Sun Y (2015) In vitro CRISPR/Cas9 system for efficient targeted DNA editing. Mbio. https://doi.org/10.1128/mBio.01714-15
Lone BA, Karna SKL, Ahmad F, Shahi N, Pokharel YR (2018) CRISPR/Cas9 system: a bacterial tailor for genomic engineering. Genetics Res Int. https://doi.org/10.1155/2018/3797214
Manguso RT, Pope HW, Zimmer MD, Brown FD, Yates KB, Miller BC et al (2017) In vivo CRISPR screening identifies Ptpn2 as a cancer immunotherapy target. Nature 547(7664):413–418
Martinez-Lage M, Torres-Ruiz R, Puig-Serra P, Moreno-Gaona P, Martin MC, Moya FJ et al (2020) In vivo CRISPR/Cas9 targeting of fusion oncogenes for selective elimination of cancer cells. Nat Commun 11(1):1–14
Matano M, Date S, Shimokawa M, Takano A, Fujii M, Ohta Y et al (2015) Modeling colorectal cancer using CRISPR-Cas9–mediated engineering of human intestinal organoids. Nat Med 21(3):256–262
Maus MV, Grupp SA, Porter DL, June CH (2014) Antibody-modified T cells: CARs take the front seat for hematologic malignancies. Blood 123(17):2625–2635
Mirza Z, Karim S (2019) Advancements in CRISPR/Cas9 technology—focusing on cancer therapeutics and beyond. Semin Cell Dev Biol 96:13–21
Modell JW, Jiang W, Marraffini LA (2017) CRISPR–Cas systems exploit viral DNA injection to establish and maintain adaptive immunity. Nature 544(7648):101–104
Moody CA, Laimins LA (2010) Human papillomavirus oncoproteins: pathways to transformation. Nat Rev Cancer 10(8):550–560
Murovec J, Pirc Ž, Yang B (2017) New variants of CRISPR RNA-guided genome editing enzymes. Plant Biotechnol J 15(8):917–926
Murphy M, Chatterjee SS, Jain S, Katari M, DasGupta R (2016) TCF7L1 modulates colorectal cancer growth by inhibiting expression of the tumor-suppressor gene EPHB3. Sci Rep 6(1):1–12
Naeem M, Majeed S, Hoque MZ, Ahmad I (2020) Latest developed strategies to minimize the off-target effects in CRISPR-Cas-mediated genome editing. Cells 9(7):1608
Nagai H, Kim YH (2017) Cancer prevention from the perspective of global cancer burden patterns. J Thorac Dis 9(3):448
Najah S, Saulnier C, Pernodet JL, Bury-Moné S (2019) Design of a generic CRISPR-Cas9 approach using the same sgRNA to perform gene editing at distinct loci. BMC Biotechnol 19(1):1–8
Nidhi S, Anand U, Oleksak P, Tripathi P, Lal JA, Thomas G et al (2021) Novel CRISPR–Cas systems: an updated review of the current achievements, applications, and future research perspectives. Int J Mol Sci 22(7):3327
Nogueira Furtado R (2019) Gene editing: the risks and benefits of modifying human DNA. Revista Bioetica 27(2):223–233
Novellasdemunt L, Foglizzo V, Cuadrado L, Antas P, Kucharska A, Encheva V et al (2017) USP7 is a tumor-specific WNT activator for APC-mutated colorectal cancer by mediating β-catenin deubiquitination. Cell Rep 21(3):612–627
O’Rourke KP, Loizou E, Livshits G, Schatoff EM, Baslan T, Manchado E et al (2017) Transplantation of engineered organoids enables rapid generation of metastatic mouse models of colorectal cancer. Nat Biotechnol 35(6):577–582
Ozates NP, Soğutlu F, Lerminoglu F, Demir B, Gunduz C, Shademan B, Avci CB (2021) Effects of rapamycin and AZD3463 combination on apoptosis, autophagy, and cell cycle for resistance control in breast cancer. Life Sci 264:118643
Ozdemir Kutbay N, Biray Avci C, Sarer Yurekli B, Caliskan Kurt C, Shademan B, Gunduz C, Erdogan M (2020) Effects of metformin and pioglitazone combination on apoptosis and AMPK/mTOR signaling pathway in human anaplastic thyroid cancer cells. J Biochem Mol Toxicol 34(10):e22547
Petersen B (2017) Basics of genome editing technology and its application in livestock species. Reprod Domest Anim 52:4–13
Pflueger C, Tan D, Swain T, Nguyen T, Pflueger J, Nefzger C, Polo JM, Ford E, Lister R (2018) A modular dCas9-SunTag DNMT3A epigenome editing system overcomes pervasive off-target activity of direct fusion dCas9-DNMT3A constructs. Genome Res 28:1193–1206
Platt RJ, Chen S, Zhou Y, Yim MJ, Swiech L, Kempton HR et al (2014) CRISPR-Cas9 knockin mice for genome editing and cancer modeling. Cell 159(2):440–455
Rath D, Amlinger L, Rath A, Lundgren M (2015) The CRISPR-Cas immune system: biology, mechanisms and applications. Biochimie 117:119–128
Ravichandran G, Rengan AK (2020) Aptamer-mediated nanotheranostics for cancer treatment: a review. ACS Appl Nano Mater 3(10):9542–9559
Reddy A, Zhang J, Davis NS, Moffitt AB, Love CL, Waldrop A et al (2017) Genetic and functional drivers of diffuse large B cell lymphoma. Cell 171(2):481–494
Ren J, Zhao Y (2017) Advancing chimeric antigen receptor T cell therapy with CRISPR/Cas9. Protein Cell 8(9):634–643
Rivenbark AG, Stolzenburg S, Beltran AS, Yuan X, Rots MG, Strahl BD, Blancafort P (2012) Epigenetic reprogramming of cancer cells via targeted DNA methylation. Epigenetics 7(4):350–360
Romero R, Sayin VI, Davidson SM, Bauer MR, Singh SX, LeBoeuf SE et al (2017) Keap1 loss promotes Kras-driven lung cancer and results in dependence on glutaminolysis. Nat Med 23(11):1362
Saadatpour Z, Rezaei A, Ebrahimnejad H, Baghaei B, Bjorklund G, Chartrand M et al (2017) Imaging techniques: new avenues in cancer gene and cell therapy. Cancer Gene Ther 24(1):1–5
Sachdeva M, Sachdeva N, Pal M, Gupta N, Khan IA, Majumdar M, Tiwari A (2015) CRISPR/Cas9: molecular tool for gene therapy to target genome and epigenome in the treatment of lung cancer. Cancer Gene Ther 22(11):509–517
Sánchez-Rivera FJ, Jacks T (2015) Applications of the CRISPR–Cas9 system in cancer biology. Nat Rev Cancer 15(7):387–393
Sanjana NE (2017) Genome-scale CRISPR pooled screens. Anal Biochem 532:95–99
Sekine R, Kawata T, Muramoto T (2018) CRISPR/Cas9 mediated targeting of multiple genes in Dictyostelium. Sci Rep 8(1):1–11
Shabbir MAB, Shabbir MZ, Wu Q, Mahmood S, Sajid A, Maan MK et al (2019) CRISPR-cas system: biological function in microbes and its use to treat antimicrobial resistant pathogens. Ann Clin Microbiol Antimicrob 18(1):21
Shademan B, Karamad V, Nourazarian A, Avci CB (2021) CAR T cells: cancer cell surface receptors are the target for cancer therapy. Adv Pharm Bull. https://doi.org/10.34172/apb.2022.051
Shalem O, Sanjana NE, Hartenian E, Shi X, Scott DA, Mikkelsen TS et al (2014) Genome-scale CRISPR-Cas9 knockout screening in human cells. Science 343(6166):84–87
Shalem O, Sanjana NE, Zhang F (2015) High-throughput functional genomics using CRISPR–Cas9. Nat Rev Genet 16(5):299–311
Shi J, Wang E, Milazzo JP, Wang Z, Kinney JB, Vakoc CR (2015) Discovery of cancer drug targets by CRISPR-Cas9 screening of protein domains. Nat Biotechnol 33(6):661–667
Siegal R, Miller KD, Jemal A (2014) Cancer statistics, 2012. Ca Cancer J Clin 64(1):9–29
Singh N, Shi J, June CH, Ruella M (2017) Genome-editing technologies in adoptive T cell immunotherapy for cancer. Curr Hematol Malig Rep 12(6):522–529
Sotiropoulos SN, Moeller S, Jbabdi S, Xu J, Andersson JL, Auerbach EJ et al (2013) Effects of image reconstruction on fiber orientation mapping from multichannel diffusion MRI: reducing the noise floor using SENSE. Magn Reson Med 70(6):1682–1689
Stadtmauer EA, Fraietta JA, Davis MM, Cohen AD, Weber KL, Lancaster E et al (2020) CRISPR-engineered T cells in patients with refractory cancer. Science 367:6481
Stolzenburg S, Beltran AS, Swift-Scanlan T, Rivenbark AG, Rashwan R, Blancafort P (2015) Stable oncogenic silencing in vivo by programmable and targeted de novo DNA methylation in breast cancer. Oncogene 34(43):5427–5435
Tanenbaum ME, Gilbert LA, Qi LS, Weissman JS, Vale RD (2014) A protein-tagging system for signal amplification in gene expression and fluorescence imaging. Cell 159(3):635–646
Tang H, Shrager JB (2016) CRISPR/Cas-mediated genome editing to treat EGFR-mutant lung cancer: a personalized molecular surgical therapy. EMBO Mol Med 8(2):83–85
Terns MP, Terns RM (2011) CRISPR-based adaptive immune systems. Curr Opin Microbiol 14(3):321–327
Tian X, Gu T, Patel S, Bode AM, Lee MH, Dong Z (2019) CRISPR/Cas9–An evolving biological tool kit for cancer biology and oncology. NPJ Precision Oncology 3(1):1–8
Torres R, Martin MC, Garcia A, Cigudosa JC, Ramirez JC, Rodriguez-Perales S (2014) Engineering human tumour-associated chromosomal translocations with the RNA-guided CRISPR–Cas9 system. Nat Commun 5(1):1–8
Vakulskas CA, Behlke MA (2019) Evaluation and reduction of CRISPR off-target cleavage events. Nucleic Acid Ther 29(4):167–174
Wang H, Sun W (2017) CRISPR-mediated targeting of HER2 inhibits cell proliferation through a dominant negative mutation. Cancer Lett 385:137–143
Wang T, Birsoy K, Hughes NW, Krupczak KM, Post Y, Wei JJ et al (2015) Identification and characterization of essential genes in the human genome. Science 350(6264):1096–1101
Wang P, Zhang L, Xie Y, Wang N, Tang R, Zheng W, Jiang X (2017) Genome editing for cancer therapy: delivery of Cas9 protein/sgRNA plasmid via a gold nanocluster/lipid core–shell nanocarrier. Adv Sci 4(11):1700175
Wang C, Jin H, Gao D, Wang L, Evers B, Xue Z et al (2018) A CRISPR screen identifies CDK7 as a therapeutic target in hepatocellular carcinoma. Cell Res 28(6):690–692
Wei C, Wang F, Liu W, Zhao W, Yang Y, Li K et al (2018) CRISPR/Cas9 targeting of the androgen receptor suppresses the growth of LNCaP human prostate cancer cells. Mol Med Rep 17(2):2901–2906
Wilkinson RA, Martin C, Nemudryi AA, Wiedenheft B (2019) CRISPR RNA-guided autonomous delivery of Cas9. Nat Struct Mol Biol 26(1):14–24
Xu Y, Li Z (2020) CRISPR-Cas systems: overview, innovations and applications in human disease research and gene therapy. Comput Struct Biotechnol J. https://doi.org/10.1016/j.csbj.2020.08.031
Yan M, Li J (2019) The evolving CRISPR technology. Protein Cell 10(11):783–786
Yang Y, Xu J, Ge S, Lai L (2021) CRISPR/Cas: advances, limitations, and applications for precision cancer research. Front Med. https://doi.org/10.3389/fmed.2021.649896
Ye L, Wang C, Hong L, Sun N, Chen D, Chen S, Han F (2018) Programmable DNA repair with CRISPRa/i enhanced homology-directed repair efficiency with a single Cas9. Cell Discovery 4(1):1–12
Yoshiba T, Saga Y, Urabe M, Uchibor R, Matsubara S, Fujiwara H, Mizukami H (2019) CRISPR/Cas9-mediated cervical cancer treatment targeting human papillomavirus E6. Oncol Lett 17(2):2197–2206
Zaboikin M, Zaboikina T, Freter C, Srinivasakumar N (2017) Non-homologous end joining and homology directed DNA repair frequency of double-stranded breaks introduced by genome editing reagents. PLoS ONE 12(1):e0169931
Zetsche B, Gootenberg JS, Abudayyeh OO, Slaymaker IM, Makarova KS, Essletzbichler P et al (2015) Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system. Cell 163(3):759–771
Zhan T, Rindtorff N, Betge J, Ebert MP, Boutros M (2019) CRISPR/Cas9 for cancer research and therapy. Semin Cancer Biol 55:106–119
Zhang XH, Tee LY, Wang XG, Huang QS, Yang SH (2015) Off-target effects in CRISPR/Cas9-mediated genome engineering. Mol Ther Nucleic Acids 4:e264
Zhang Z, Chen J, Zhu Z, Zhu Z, Liao X, Wu J et al (2021) CRISPR-Cas13-mediated knockdown of lncRNA-GACAT3 inhibited cell proliferation and motility, and induced apoptosis by increasing p21, Bax, and E-cadherin expression in bladder cancer. Front Mol Biosci 7:433
Zhao G, Wang Q, Gu Q, Qiang W, Wei JJ, Dong P et al (2017) Lentiviral CRISPR/Cas9 nickase vector mediated BIRC5 editing inhibits epithelial to mesenchymal transition in ovarian cancer cells. Oncotarget 8(55):94666
Zhao X, Liu L, Lang J, Cheng K, Wang Y, Li X et al (2018) A CRISPR-Cas13a system for efficient and specific therapeutic targeting of mutant KRAS for pancreatic cancer treatment. Cancer Lett 431:171–181
Zhao Z, Li C, Tong F, Deng J, Huang G, Sang Y (2021) Review of applications of CRISPR-Cas9 gene-editing technology in cancer research. Biol Proced Online 23(1):1–13
Zhen S, Hua L, Takahashi Y, Narita S, Liu YH, Li Y (2014) In vitro and in vivo growth suppression of human papillomavirus 16-positive cervical cancer cells by CRISPR/Cas9. Biochem Biophys Res Commun 450(4):1422–1426
Zheng J, Xiong D, Sun X, Wang J, Hao M, Ding T et al (2012) Signification of hypermethylated in cancer 1 (HIC1) as tumor suppressor gene in tumor progression. Cancer Microenviron 5(3):285–293
Zou F, Mao R, Yang L, Lin S, Lei K, Zheng Y et al (2016) Targeted deletion of miR-139-5p activates MAPK, NF-κB and STAT 3 signaling and promotes intestinal inflammation and colorectal cancer. FEBS J 283(8):1438–1452
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Shademan, B., Masjedi, S., Karamad, V. et al. CRISPR Technology in Cancer Diagnosis and Treatment: Opportunities and Challenges. Biochem Genet 60, 1446–1470 (2022). https://doi.org/10.1007/s10528-022-10193-9
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DOI: https://doi.org/10.1007/s10528-022-10193-9