1,642
Views
7
CrossRef citations to date
0
Altmetric
Review

A novel fiber chimeric conditionally replicative adenovirus-Ad5/F35 for tumor therapy

, , , , , , , , & show all
Pages 833-840 | Received 20 Mar 2017, Accepted 13 Oct 2017, Published online: 16 Nov 2017

Figures & data

Figure 1. Schematic diagrams of the Ad5 vectors and Ad5/F35.

Figure 1. Schematic diagrams of the Ad5 vectors and Ad5/F35.

Figure 2. The mechanism of the antitumor effect of vectors incorporating the novel chimeric fiber Ad5/F35 adenovirus. Ad5/F35 first attaches to cells via CD46 or CAR. Once attached, the RGD motif in the penton base interacts with integrin to promote endocytosis and internalization of the adenovirus. Ad5/F35 then lyses the tumor cells via apoptosis. The released adenoviruses infect adjacent tumor cells.

Figure 2. The mechanism of the antitumor effect of vectors incorporating the novel chimeric fiber Ad5/F35 adenovirus. Ad5/F35 first attaches to cells via CD46 or CAR. Once attached, the RGD motif in the penton base interacts with integrin to promote endocytosis and internalization of the adenovirus. Ad5/F35 then lyses the tumor cells via apoptosis. The released adenoviruses infect adjacent tumor cells.

Table 1. Factors influencing the transduction efficacy of Ad5/F35 vectors.

Table 2. Studies using Ad5/F35-based vectors in various cancers.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.