Literature DB >> 27832705

AAV Infection: Protection from Cancer.

Arun Srivastava1, Barrie J Carter2.   

Abstract

There are conflicting reports that integration of the wild-type adeno-associated virus 2 (AAV2) genome is associated with induction of hepatocellular carcinoma (HCC) in a small subset of patients. However, there are several lines of evidence that contradict this assertion: (i) AAV2 has long been known to be a non-pathogenic virus, although ∼90% of the human population is seropositive for AAV2 antibodies; (ii) AAV2 has been shown to possess anticancer activity; (iii) epidemiological evidence suggests that AAV2 infection plays a protective role against cervical carcinoma; and (iv) five different AAV serotype vectors (AAV1, AAV2, AAV5, AAV8, and AAV9) have been or are currently being used in 162 Phase I/II clinical trials and one Phase III clinical trial in humans to date, and no cancer of any type has ever been observed or reported. A brief historical account of the putative role of infection by AAV in the etiology of cancer, or lack thereof, is presented.

Entities:  

Keywords:  DNA integration; liver cancer; recombinant AAV vectors; wild-type AAV2

Mesh:

Year:  2016        PMID: 27832705      PMCID: PMC5399746          DOI: 10.1089/hum.2016.147

Source DB:  PubMed          Journal:  Hum Gene Ther        ISSN: 1043-0342            Impact factor:   5.695


  70 in total

1.  Long-term correction of inhibitor-prone hemophilia B dogs treated with liver-directed AAV2-mediated factor IX gene therapy.

Authors:  Glenn P Niemeyer; Roland W Herzog; Jane Mount; Valder R Arruda; D Michael Tillson; John Hathcock; Frederik W van Ginkel; Katherine A High; Clinton D Lothrop
Journal:  Blood       Date:  2008-10-28       Impact factor: 22.113

2.  Influence of adeno-associated satellite virus on adenovirus-induced tumours in hamsters.

Authors:  H D Mayor; G S Houlditch; D M Mumford
Journal:  Nat New Biol       Date:  1973-01-10

3.  Molecular structure of adeno-associated virus variant DNA.

Authors:  L M de la Maza; B J Carter
Journal:  J Biol Chem       Date:  1980-04-10       Impact factor: 5.157

4.  Altered biology of adeno-associated virus type 2 and human papillomavirus during dual infection of natural host tissue.

Authors:  C Meyers; S Alam; M Mane; P L Hermonat
Journal:  Virology       Date:  2001-08-15       Impact factor: 3.616

5.  The adeno-associated virus Rep78 gene inhibits cellular transformation induced by bovine papillomavirus.

Authors:  P L Hermonat
Journal:  Virology       Date:  1989-09       Impact factor: 3.616

6.  Inhibition/stimulation of bovine papillomavirus by adeno-associated virus is time as well as multiplicity dependent.

Authors:  P L Hermonat; C Meyers; G P Parham; A D Santin
Journal:  Virology       Date:  1998-08-01       Impact factor: 3.616

7.  Recombinant AAV Integration Is Not Associated With Hepatic Genotoxicity in Nonhuman Primates and Patients.

Authors:  Irene Gil-Farina; Raffaele Fronza; Christine Kaeppel; Esperanza Lopez-Franco; Valerie Ferreira; Delia D'Avola; Alberto Benito; Jesus Prieto; Harald Petry; Gloria Gonzalez-Aseguinolaza; Manfred Schmidt
Journal:  Mol Ther       Date:  2016-03-07       Impact factor: 11.454

8.  Adeno-associated virus finds its disease.

Authors:  David W Russell; Markus Grompe
Journal:  Nat Genet       Date:  2015-10       Impact factor: 38.330

9.  Antibodies to adeno-associated satellite virus and herpes simplex in sera from cancer patients and normal adults.

Authors:  H D Mayor; S Drake; J Stahmann; D M Mumford
Journal:  Am J Obstet Gynecol       Date:  1976-09-01       Impact factor: 8.661

10.  The regulatory rep protein of adeno-associated virus binds to sequences within the c-H-ras promoter.

Authors:  R B Batchu; R M Kotin; P L Hermonat
Journal:  Cancer Lett       Date:  1994-10-28       Impact factor: 8.679

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  13 in total

Review 1.  Gene therapy for hemophilia: what does the future hold?

Authors:  Bhavya S Doshi; Valder R Arruda
Journal:  Ther Adv Hematol       Date:  2018-08-27

Review 2.  AAV: An Overview of Unanswered Questions.

Authors:  Kenneth I Berns; Nicholas Muzyczka
Journal:  Hum Gene Ther       Date:  2017-04       Impact factor: 5.695

3.  A directed evolution approach to select for novel Adeno-associated virus capsids on an HIV-1 producer T cell line.

Authors:  Dawn P Wooley; Priyanka Sharma; John R Weinstein; Poornima Kotha Lakshmi Narayan; David V Schaffer; Katherine J D A Excoffon
Journal:  J Virol Methods       Date:  2017-09-14       Impact factor: 2.014

4.  A Tribute to Barrie J. Carter.

Authors:  Arun Srivastava; Matthew Weitzman; Saswati Chatterjee; John F Engelhardt; Roland A Owens; Nick Muzyczka; Robin Ali
Journal:  Hum Gene Ther       Date:  2020-04-02       Impact factor: 5.695

5.  Recombinant Adeno-Associated Virus Gene Therapy in Light of Luxturna (and Zolgensma and Glybera): Where Are We, and How Did We Get Here?

Authors:  Allison M Keeler; Terence R Flotte
Journal:  Annu Rev Virol       Date:  2019-07-05       Impact factor: 10.431

6.  Human Bocavirus 1 Is a Novel Helper for Adeno-associated Virus Replication.

Authors:  Zekun Wang; Xuefeng Deng; Wei Zou; John F Engelhardt; Ziying Yan; Jianming Qiu
Journal:  J Virol       Date:  2017-08-24       Impact factor: 5.103

Review 7.  Evaluating the state of the science for adeno-associated virus integration: An integrated perspective.

Authors:  Denise E Sabatino; Frederic D Bushman; Randy J Chandler; Ronald G Crystal; Beverly L Davidson; Ricardo Dolmetsch; Kevin C Eggan; Guangping Gao; Irene Gil-Farina; Mark A Kay; Douglas M McCarty; Eugenio Montini; Adora Ndu; Jing Yuan
Journal:  Mol Ther       Date:  2022-06-10       Impact factor: 12.910

Review 8.  A Systematic Review and Meta-Analyses of Interventional Clinical Trial Studies for Gene Therapies for the Inherited Retinal Degenerations (IRDs).

Authors:  Gearóid P Tuohy; Roly Megaw
Journal:  Biomolecules       Date:  2021-05-19

Review 9.  Biomaterial-guided delivery of gene vectors for targeted articular cartilage repair.

Authors:  Magali Cucchiarini; Henning Madry
Journal:  Nat Rev Rheumatol       Date:  2019-01       Impact factor: 20.543

10.  CRISPR/Cas9-mediated genome editing via postnatal administration of AAV vector cures haemophilia B mice.

Authors:  Tsukasa Ohmori; Yasumitsu Nagao; Hiroaki Mizukami; Asuka Sakata; Shin-Ichi Muramatsu; Keiya Ozawa; Shin-Ichi Tominaga; Yutaka Hanazono; Satoshi Nishimura; Osamu Nureki; Yoichi Sakata
Journal:  Sci Rep       Date:  2017-06-23       Impact factor: 4.379

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