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©2014 Baishideng Publishing Group Inc.
World J Gastroenterol. Oct 7, 2014; 20(37): 13343-13368
Published online Oct 7, 2014. doi: 10.3748/wjg.v20.i37.13343
Published online Oct 7, 2014. doi: 10.3748/wjg.v20.i37.13343
Table 1 Comparison of characters of common viral vectors
| Virus | Viral genome | Insertion capacity | Host range of infection | State of integration into host genome | Efficiency of gene transfection and expression | Immunogenicity | Titers of preparation in vitro(PFU/mL) | Bio-safety |
| AdV | Double-stranded DNA | 38 kb | Broad spectrum (both dividing and non-dividing cells) | No integration | High | High | 1011-1012 | Safe |
| AAV | Single-stranded DNA | 4.9 kb | Broad spectrum | Site-specific integration on chromosome 19q13.3 | High | Low | 1012, dependent on helper virus | Safe |
| RV | Single-stranded RNA | 8 kb | Dividing cells only | Integrate randomly | Low | Low | 106-107 | Risk of insertional mutagenesis |
| Lentivirus | Single-stranded RNA | 8 kb | Broad spectrum | Integrate randomly | High | Low | 109-1010 | Risk of viral infection and insertional mutagenesis |
| Pox virus | Souble-stranded DNA | 25 kb | Broad spectrum | No integration | High | High, function as immunologic adjuvant | 106-107 | Safe |
| HSV | Double-stranded DNA | 15-30 kb | Nerve cells and epithelial cells, especially neuro- tropic speciality | No integration | High | Moderate | 1011-1012 | Risk of viral infection |
Table 2 Target genes of gene therapy in pancreatic cancer
| Strategy | Categories | Examples |
| Gene augumentation | Tumor suppressor genes | p16INK4a, p21CIP1/WAF1, p14ARF, Retinoblastoma Protein (pRb), p53, p84 /Thoc1, p73, Smad4/DPC4 |
| Drug sensitivity genes/ suicide genes | Herpes Simplex Virus Thymidine Kinase (HSV-TK), Cytosine Deaminase (CD), Nitroreductase (NTR), Cytochrome P450 (CYP) | |
| Anti-angiogenesis genes | Soluble VEGFR, Soluble FGFR, Endostatin, Thrombospondin-1, Angiostatin, Vasostatin, NK4, Matrix metalloproteinases inhibitors (MMIPs/TIMPs), Somatostatin receptors (SSTR) | |
| Immune related genes | MHC molecules, Co-stimulatory molecules (B7 family, ICAM-1, LFA-3), Inflammatory cytokines (IL-2, IL-12, GM-CSF, IFN-α, IFN-β, IFN-γ, TNF-α), Tumor antigen (CEA, MUC-1, etc.) | |
| Apoptosis related genes | TRAIL | |
| Gene blockade/antisense therapy | Oncogenes | K-ras, LSM1/CaSm, HER-2/EerB-2 |
| MDR | MDR1, MRP family, BCRP | |
| Proliferation related genes | VEGF, hTERT, COX-2 |
Table 3 Active and negative regulatory factors of angiogenesis
| Stimulators | Inhibitors |
| Hypoxia | Angiostatin |
| Oncogenic proteins such as Ras | TSP-1 |
| Inflammatory cytokines such as IL-8 and IL-6 | Endostatin |
| FGF | Arrestin |
| TGF-β | Canstatin |
| HGF | MMPIs |
| PDGF | Somatostatin |
| G-CSF | Tumstatin |
| Angiogenin | VEGI |
| Leptin | Decoy receptors such as soluble VEGFR |
| Proliferin | Inflammatory cytokines such as IL-12 |
Table 4 Antigenic sources used in pancreatic cancer vaccine trials
| Peptide or protein vaccines | Mutant K-ras peptide |
| WT1 peptide | |
| CAP1-6D | |
| G17DT | |
| HLA-A*0201 restricted VEGF receptor-1 and -2 peptides | |
| HLA-A24 restricted survivin-2B80-88 peptide (AYACNTSTL) | |
| Autologous heat shock protein HSPPC-96 | |
| TELOVAC | |
| Whole cell vaccines or dendritic cell vaccines | α-Gal transferase transfected allogeneic tumor cells (including Algenpantucel-L) |
| GVAX | |
| MUC-1 pulsed autologous dendritic cells | |
| Viral or bacterial vaccines | PANVAC-VF-MUC-1, CEA, and TRICOM transfected virus |
| Mesothelin (CRS-207) transfected live-attenuated Listeria | |
| DNA vaccines | VXMO1 |
Table 5 Closed clinical trials of gene therapy in pancreatic cancer
| Trial ID and investigator | Phase | Clinical indication | Patients(n) | Transgenes | Vectors and target cells | Administration route | Combined therapy | Results |
| DE-0009 Löhr et al[67] | I/II | Inoperable PC | 14 | Cytochrome p450 | Naked/plasmid DNA transfected allogeneic human 293 embryonic kidney cells | Inject into the tumor vasculature via supraselective angiography | In combination with low-dose ifosfamide | 4 patients showed tumor regression, the other ten individuals remained stable. Median survival was doubled compared with historic controls. 1-yr survival rate was three times better |
| DE-0024 Pecher et al[207] | I/II | Advanced breast cancer, PC and gallbladder carcinoma | 10 (2 PC) | MUC-1 | Naked/plasmid DNA transfected autologus dendritic cells | Subcutaneous injection | None | 9 patients showed signs of progression. Only one remained stable for 3 mo until she was transferred to another therapy. 3 of 10 patients developed vaccine-specific delayed-type hypersensitivity reaction (DTH). 4 of 10 patients showed increased mucinspecific INF-gamma- secreting CD8+ T cells |
| DE-0063 Kubuschok et al[208] | I | PC | 3 healthy donors and 1 PC patient | Mutated ras oncoprotein | EB virus transformed autologous lymphoblastoid cells | Subcutaneous injection | None | All the subjects showed strong vaccine-induced muRas-specific cytotoxic T lymphocytes |
| DE-0083 Niethammer et al[209] | I | Advanced PC | 45 | VEGFR-2 | Naked/plasmid DNA (oral DNA vaccine) | Oral administration | In combination with gemcitabine | Not reported |
| ES-0004 Mazzolini et al[210] | I | Liver cancer, PC, colorectal cancer | 17 (3 PC) | Interleukin-12 (IL-12) | Adenovirus transfected autologous dendritic cells | Intratumoral injection | None | Treatment was well tolerated. 11 of 17 were assessable for response. A partial response was observed in 1 case with PC. Stable disease was observed in 2 patients and progression in 8 patients |
| FR-0018 Gilly et al[211] | I/II | Unresectable digestive cancer | 6 (3 PC) | Interleukin-2 (IL-2) | Adenovirus | Intratumoral injection | None | Good safety. But final results of tumor responses were not reported |
| US-0853 Le et al[212] | I | Ovarian cancer, PC, lung cancer, mesothelioma | 28 | Mesothelin | Listeria monocytogenes | Intravenous injection | 1: Live attenuated Listeria vaccine (n = 9); 2: live attenuated mesothein expressing Listeria vaccine ( n = 17) | In arm 2, Listeriolysin O and mesothelin-specific T-cell responses were seen and 37% of subjects lived ≥ 15 mo |
| US-0700 Galanis et al[213] | I | Gemcitabine-refractory, metastatic PC | 12 | Cyclin G1 | Retrovirus | Intravenous injection | None | Good safety. But there was no evidence of anti-tumor activity |
| Kaufman et al[214] | I | Advanced PC | 10 | CEA, MUC-1, and TRICOM (including B7.1, ICAM-1, LFA-3) | Poxvirus | Subcutaneous injection | In combination with GM-CSF | Antigen-specific T-cell responses in 5 of 8 evaluated patients. 15.1 mo of median survival in responders vs 3.9 mo in non-responders. Overall median survival is 6.3 mo |
| Jaffee et al[141] | I | Resected PC | 14 | GM-CSF | Naked/plasmid DNA transfected allogeneic tumor cell vaccine | Intradermal injection | In combination with standard chemoradiation | 3 of 14 patients developed DTH, and 3 patients had increased disease-free survival time (at least 25 mo after diagnosis) |
| US-0475 Lutz et al[215] | II | Resected PC | 60 | GM-CSF | Naked/plasmid DNA transfected allogeneic tumor cell vaccine | Intradermal injection | In combination with standard chemoradiation | The median disease-free survival is 17.3 mo with median survival of 24.8 mo. Induction of CD8+ mesothelin-specific T cells correlated with disease-free survival |
| Laheru et al[142] | A pilot study | Advanced PC | 50 | GM-CSF | Naked/plasmid DNA transfected allogeneic tumor cell vaccine | Intradermal injection | A: vaccine alone (n = 20) B: vaccine plus cyclophosphamide (n = 30) | Cohort B showed enhanced mesothelin-specific T-cell responses. Median survival values in cohort A and cohort B were 2.3 and 4.3 mo |
| Le et al[143] | Ib | Advanced PC | 30 | CM-CSF | Naked/plasmid DNA transfected allogeneic tumor cell vaccine | Intradermal injection | 1: Ipilimumab alone (n = 15); 2: Ipilimumab plus vaccine (n = 15) | Median overall survival was 3.6 mo for arm 1 and 5.7 mo for arm 2. Mesothelin-specific T cells responses were associated with increased disease-free survival in arm 2 |
Table 6 Ongoing clinical trials of gene therapy in pancreatic cancer
| Phase | Transgenes |
| I | Oncolytic adenovirus and oncolytic herpesvirus1 |
| Somatostatin receptor 2 (sst2), Deoxycitidine kinase :: uridylmonophosphate kinase (dck::umk) | |
| Somatostatin receptor 2 (sst2) | |
| Mesothelin-scFv with signaling domains comprised of TCR , CD28, and 4-1BB (CD137) cDNA | |
| GM-CSF | |
| PANVAC (CEA, MUC-1, and TRICOM) | |
| Cytosine deaminase, Herpes simplex virus thymidine kinase (HSV-TK) | |
| Cyclin G1 | |
| p53 | |
| BikDD (DOTAP-cholesterol mediated gene transfection) | |
| Mutated Ras | |
| I/II | Cytochrome p450 |
| AEG 35156: antisense oligonucleotide to X-linked inhibitor of apoptosis protein (XIAP) | |
| Herpes simplex virus thymidine kinase (HSV-TK) | |
| Diphtheria Toxin A Chain (DTA) gene with H19 promoter | |
| Alpha-(1,3) galactosyltransferase | |
| II | CEA, MUC-1, and PANVAC |
| Mutated Ras | |
| Alpha-(1,3) galactosyltransferase | |
| III | Alpha-(1,3) galactosyltransferase |
| PANVAC (CEA, MUC-1, and TRICOM)2 |
Table 7 Clinical trials of unspecific tumor gene therapy that may involve pancreatic cancer
| Phase | Clinical indication | Transgenes |
| II | Adenocarcinoma | CEA, TCRzeta and CD28 |
| I | Cachexia | GHRH |
| I | CEA- or HER-2-expressing malignancies | HER-2, CEA |
| I | CEA-expressing malignancies | CEA |
| I/II | CEA-expressing malignancies | CAP-1 peptide from CEA |
| I/II | CEA-expressing malignancies | T cell receptor alpha and beta chains cDNA |
| I | CEA-expressing malignancies | CEA, B7.1, ICAM-1, LFA-3, GM-CSF |
| I | CEA-expressing malignancies | Anti-CEA-SFv-Zeta T cell receptor |
| I | CEA-expressing malignancies | B7.1 (CD80) |
| II | Advanced cancer with overexpression of p53 | Anti-p53 T cell receptor |
| I | MUC-1- expressing tumors | MUC-1, IL-2 |
| I | Advanced cancer | Cytochrome P450 |
| I | Advanced cancer | Endostatin |
| I | Advanced cancer | Heat shock protein 70 |
| I | Advanced cancer | T cell receptor alpha and beta chain |
| I | Advanced cancer | Bifunctional shRNA specific for stathmin 1 oncoprotein |
| I/II | Advanced cancer | GM-CSF |
| I | Advanced cancer | IL-12 |
| I/II | Advanced cancer | CYP1B1 |
| I | Advanced cancer | GM-CSF, CD154 (CD40-ligand) |
| I/II | Advanced cancer | IL-2 |
| I | Advanced cancer | p53 |
| I | Advanced cancer | AMEP |
| I | Advanced cancer | B7.1 (CD80) ,ICAM-1, LFA-3 |
| I/II | Advanced cancer | Cytosine deaminase |
| I/II | Advanced cancer | CEA |
| I | Solid tumors | Tumor antigen |
| I | Solid tumors | Interferon-gamma |
| I | Solid tumors | TNF |
| I | Solid tumors | Brachyury oncoprotein |
| I | Solid tumors | Human telomerase reverse transcriptase |
| I/II | Solid tumors | Oncolytic virus (no transgene) |
| I | Solid tumors | Retinoblastoma 94 |
| I | Solid tumors | p53 |
| I | Solid tumors | O6-methylguanine DNA methyltransferase (MGMT) |
| I | Solid tumors | GM-CSF |
| I | Solid tumors | GM-CSF, bi-shRNA-furin |
| I | Solid tumors | GM-CSF, TGF-beta 2 antisense |
| I | Solid tumors | GM-CSF, humanized Escherichia coli beta-galactosidase |
- Citation: Liu SX, Xia ZS, Zhong YQ. Gene therapy in pancreatic cancer. World J Gastroenterol 2014; 20(37): 13343-13368
- URL: https://www.wjgnet.com/1007-9327/full/v20/i37/13343.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i37.13343
