2020
DOI: 10.1080/17425247.2020.1747429
|View full text |Cite
|
Sign up to set email alerts
|

Delivery of genome editing tools: A promising strategy for HPV-related cervical malignancy therapy

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
21
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
10

Relationship

2
8

Authors

Journals

citations
Cited by 26 publications
(22 citation statements)
references
References 137 publications
1
21
0
Order By: Relevance
“…ZFNs targeting HPV16 and 18 induced in vitro E7 interruption and inhibition of type-specific and efficient growth and apoptosis of HPV-positive cells. These targeted ZFNs may be possible new therapeutic agents for the treatment of HPV-related cervical cancer [ 151 , 152 , 153 ].…”
Section: Immunotherapymentioning
confidence: 99%
“…ZFNs targeting HPV16 and 18 induced in vitro E7 interruption and inhibition of type-specific and efficient growth and apoptosis of HPV-positive cells. These targeted ZFNs may be possible new therapeutic agents for the treatment of HPV-related cervical cancer [ 151 , 152 , 153 ].…”
Section: Immunotherapymentioning
confidence: 99%
“…HPV is an oncovirus that causes several cancers, like anal, genital, and oropharyngeal cancers, and elevates the risks of dysplasia and cervical malignancy [129]. HPV is known to induce vagina mucosal infection, mucosal immunity and inflammations via several mechanisms like the induction of interferon, activation of macrophages and NK cells stimulation.…”
Section: Human Papilloma Virus (Hpv)mentioning
confidence: 99%
“…Although there are some serious drawbacks like immune response stimulation and introducing undesirable genetic mutations, due to high efficacy, viral vectors are the most common systems for not only in vivo but also in vitro plasmid delivery to mammalian cells. Various virus‐based delivery systems including retrovirus, herpes simplex virus (HSV), adenovirus, adeno‐associated virus (AAV), and lentivirus have been used for in vivo gene therapy in ND [88, 89].…”
Section: Viral‐based Deliverymentioning
confidence: 99%