The Practical Consideration of Poliovirus as an Oncolytic Virotherapy

Introduction

Risks and Benefits of Current Cancer Treatments

Current cancer treatment is dominated by chemotherapy, radiation therapy and surgery. Cancer treatments are directed to target mild cancers, or to prolong the survival time and preserve the quality of life in patients with advanced disease (Chan and McFadden, 2014; Siegel et al., 2012). Overall, 5-year cancer survival rates have increased over the past 40 years (Siegel et al., 2012). For instance, breast cancer survival rates have increased from 75.1 to 90%, childhood cancer survival rates have increased from 58.1 to 82.5% and Hodgkin’s Lymphoma survival rates have increased from 72.0 to 86.3% (Siegel et al., 2012).

Chemotherapy uses cytotoxic agents most often given intravenously to slow growth or kill rapidly dividing cells. While rapid division is a characteristic of cancer cells, other cells in the human body, including those in the bone marrow, gastrointestinal system and hair follicles also divide rapidly. These noncancerous mitotic cells are therefore often casualties of anticancer chemotherapies (Sugerman, 2013). Due to this collateral damage, common side effects associated with chemotherapy include reduced bone density, cognitive deficits including change in concentration, memory and mental speed and fatigue (Siegel et al., 2012). Other side effects include infertility, impaired pulmonary function (Siegel et al., 2012), nausea and vomiting (Rapoport et al., 2015), peripheral neuropathy and pain (Reyes-Gibby et al., 2015; Siegel et al., 2012), neutropenia and associated immunosuppression (Hashiguchi et al., 2015), cardiotoxicity (Siegel et al., 2012) and sexual dysfunction. Radiation therapy and surgery target cancer tissue more specifically. Radiation therapy uses different types of high-energy radiation delivered either externally via a smachine or internally via a radioactive material to kill target cancer cells by initiating DNA damage. This damage prevents the cell from replicating effectively which eventually causes cell death. This type of treatment can also damage cells in the surrounding area (Baskar et al., 2012). Common side effects of radiation therapy include diarrhea, fatigue, mucositis, skin toxicity and xerostomia (Stubbe and Valero, 2013).

Surgery as a form of treatment is even more localized and aims to remove the cancerous tissue directly. While this is the most confined of the treatments, surgery is also the most invasive (Chi et al., 2014; Goldfarb et al., 2010). Surgical treatment complications include lymphedema, pain, bowel complications, incontinence, sexual dysfunction and impaired lung function (Siegel et al., 2012).

More recently, recombinant virotherapy has emerged as an alternative to standard anti-cancer therapies. The objective of this literature review is to collect relevant information regarding the innovative process of virotherapy development, the current application of this therapy and the possibility of future use. Relevant articles were retrieved from the PubMed database. The novelty of this topic limited us to review those articles that were published between 2002 and the date of the submission of this manuscript. References lists were also reviewed to retrieve supplementary articles. Included articles encompass both primary and secondary literature

Despite advances in chemotherapy, radiation and surgery, cancer continues to be a top cause of death worldwide. Therefore, it is appropriate for the healthcare community to explore diverse options of cancer treatment. The use of oncolytic virotherapy shows encouraging results for applicable clinical use in cancer treatment for future cancer patients

Main Text

A Brief History of Oncolytic Virotherapy

The linkage of viral discovery to therapeutic treatment began in 1904, when Dr. George Dock hypothesized that viruses could be beneficial (Larson et al., 2015). This premise was founded on a case report of a female leukemia patient who entered a period of remission after undergoing an active infection with the influenza virus (Larson et al., 2015). In the 1950’s, additional case reports amassed, including a vignette about a cervical cancer patient who showed tumor size reduction after being injected with an attenuated rabies virus as a precautionary treatment for a dog bite (Larson et al., 2015). These case reports initiated clinical trials with attenuated viruses for the purpose of cancer treatment. A variety of viruses were used in these trials, including adenoviruses, hepatitis, yellow fever and West Nile, among others, but since the standards of clinical trials are not comparable to those of scientific research today the success of these clinical trials is difficult to ascertain (Larson et al., 2015). As technology continued to progress, specifically genetic engineering, the possibility exists for an array of viruses to be manipulated and subsequently adapted for clinical use (Larson et al., 2015).

The Premise of Oncolytic Virotherapy

The practice of oncolytic virotherapy includes selecting a virus that meets defined criteria for safety and efficacy in humans. First, the virus must exhibit selectivity for cancer cells, while avoiding normally functioning human cells. Some viruses have the innate ability to target cancer cells, such as human orphan viruses (viruses not associated with disease) and animal viruses that lack specificity for human cells, like the myxoma virus (Goetz and Gromeier, 2010). Other viruses, including poliovirus, adenovirus and herpes simplex virus, have the natural ability to target cancer cells, but must be genetically modified to remove virulence potential and protect the safety of the host (Goetz and Gromeier, 2010). For oncolytic polioviruses, this was accomplished in part by replacing an intrinsic genetic component critical for viral protein translation (IRES element) with an equivalent component of human rhinovirus type 2. This change prohibited viral replication in normal neuronal cells, but supported replication in tumors of the central nervous system and elsewhere (Goetz and Gromeier, 2010).

Secondly, the recombinant virus must be genetically stable and be incapable of reverting back to its wild-type form while replicating inside tumor cells (Brown et al., 2014). In addition, the genetically modified virus must effectively destroy tumor cells and evade or remain functional during immune responses (Brown et al., 2014). Oncolytic viruses must be able to bind to and infect target cancer cells. The poliovirus naturally binds to CD155 (Necl-5, nectin-like molecule 5) which is expressed in abundance on many malignant cancer cells (Brown et al., 2014). Virotherapies have been administered in a number of routes experimentally over the years (Southam, 1960). Recent studies with recombinant polioviruses indicate that direct intratumoral administration is promising. After administration and viral entry, replication ensues within the cancerous cells which leads to tumor cell lysis and death (Goetz and Gromeier, 2010; Brown et al., 2014). Newly replicated viruses freely invade additional local tumor cells and can circulate to metastatic cells elsewhere in the body, repeating the replication-lysis process (Sze et al., 2013).

The host immune response is critical for the success of oncolytic virotherapies (Brown et al., 2014). The type 1 interferons, INFα and β, are cytokines produced in response to viral infections (Brown et al., 2014). These molecules normally lead to a cascade of events aimed to limiting viral replication. However, antiviral responses are often inadequate in cancerous cells, limiting the effectiveness of these cytokines to initiate viral clearance (Brown et al., 2014). Conversely, type 1 interferons are important for the development of anti-cancer adaptive immunity, a scenario that benefits the efficacy of oncolytic virotherapies (Brown et al., 2014).

Normal Infectious Processes of Polioviruses

The poliovirus is a small, single stranded RNA virus with an icosahedral protein coat that causes disease in both animals and humans (Kotla and Gustin, 2015). This virus is inhaled through the nasal and pharyngeal passageways and multiplies rapidly in the epithelial cells within the pharynx and GI tract. Infection is initiated upon viral attachment of capsid proteins VP1, VP2 and VP3 to CD155 receptors on host cells. Subtle conformational changes take place within the major viral capsid proteins (VP1, VP2 and VP3) that allow the virus to attach to the membrane, create a pore and release the viral RNA into the cytoplasm. The viral RNA is then replicated and translated to synthesize viral proteins within the host cell. Translation results in a polyprotein that is then configured into multiple intermediate forms before ultimately producing the infectious virus form known as a virion. These viral proteins also produce another capsid for the virus to exit and infect nearby host cells as a virion (Hogle, 2002).

Viral RNA is recognized in infected cells by receptors both on the membrane and in the cytoplasm of the host cells. These receptors include TLRs and RIGlike receptors, RIG-I and MDA-5 (Hogle, 2002). Once viral RNA is recognized via RIG-like receptors, cellular signaling leads to activation of specific transcription factors, one being IRF-3 which activates the type I interferon response. The activation of the type I interferon response play a key role in slowing disease progression and spread. Poliovirus contains many mechanisms to inhibit this type I interferon response. For instance, poliovirus blocks the activation of IRF-3 thereby inhibiting the type I interferon response. Studies suggest the virus modulates stress granules formed in cellular cytoplasm in response to a viral infection which in turn may contribute to blocking IRF-3 activation (Kotla and Gustin, 2015).

Mechanism and Therapeutic Benefit of PVSRIPO

Through genetic manipulation, polioviruses have been engineered to be highly attenuated to ensure safety and proper oncolytic function (Goetz et al., 2011). One such recombinant poliovirus, the polio: Rhinovirus chimera (PVSRIPO) has shown promise for glioblastoma treatment. To attenuate PVSRIPO, the Internal Ribosomal Entry Site (IRES) of the PVSRIPO was substituted with the IRES from Human Rhinovirus type 2 (HRV2), which is an enterovirus specific to the respiratory system. The IRES is a nucleotide sequence located within the middle segment of messenger RNA (mRNA) used to initiate translation. These IRES elements are features paramount to viral protein synthesis. Changing the IRES of the PVSRIPO allows this recombinant virus to replicate in transformed or cancerous cells. However, the HRV2 IRES precludes replication in normal neurons, preventing adverse neural effects, but still rendering the PVSRIPO cytotoxic to cancer cells (Goetz and Gromeier, 2010; Brown and Gromier, 2015; Goetz et al., 2011). Specifically, attenuation of the IRES causes an inability of the PVSRIPO mRNA to recruit eukaryotic Initiation Factor 4G (eIF4G). Lack of eIF4G recruitment, which is a capbinding protein that bridges ribosomal subunits to initiate protein synthesis, prevents viral protein translation which causes the attenuated PVSRIPO to be non-cytolytic in the central nervous system cells of the host (Goetz et al., 2011). This attenuation of PVSRIPO in normal host cells allows for the specificity of cytotoxicity in cancerous tissue.

Many attributes of PVSRIPO make this virus capable of lysing cancerous cells but incapable of infecting and replicating in non-malignant host cells (Brown and Gromier, 2015). PVSRIPO has a natural affinity for CD155 antigens, which are specific surface markers abundant on glioblastoma cells. CD155 is also expressed on antigen presenting cells such as dendritic cells and macrophages (Brown et al., 2014). Unlike cancer cells that have a weakened antiviral response, macrophages and dendritic cells exposed to PVSRIPO are capable of limiting viral replication and can engage T cells (Brown et al., 2014). PVSRIPO has potential to be used as a treatment against a multitude of cancers as many diverse tumor cells exhibit abundant surface expression of CD155 (Brown et al., 2014; Merrill et al., 2004). The PVSRIPO affinity for CD155 coupled with the attenuation of this virus- which blocks the viral cytotoxicity in normal host cells- are central to the selectivity of cancerous tissue by this virotherapy.

Many cancers can suppress immune responses, thereby prolonging the longevity of the associated disease. PVSRIPO has the ability to activate the host innate immune response within tumor cells, even those that elicit immunosuppression (Brown and Gromier, 2015). In addition to viral molecules activating type I interferons, this is also accomplished by the PVSRIPOinduced lysis of tumor cells which leads to the release of Danger-Associated Molecular Patterns (DAMPs) that activate inflammatory responses. Moreover, tumor cell lysis results in the exposure of tumor antigens to antigen presenting cells and subsequently the adaptive immune response (Brown et al., 2014). These adaptive responses include activation of NK and Th1 cells, which target and destroy the tumor cells (Goetz et al., 2011).

Current Application

Oncolytic virotherapy using PVSRIPO has been experimentally successful in targeting glioblastoma and neuroblastoma cells, but has been ineffective in the treatment of Burkitt’s Lymphoma (Toyoda et al., 2007; Gromeier et al., 2014). The use of polioviruses to treat neuroblastoma in mice yielded favorable results, identifying the possibility for clinical application for similar types of cancers, especially those prominent in childhood. Neuroblastoma is one of the most frequent cancers in children and treatment is invasive and of high risk with poor outcomes, so the use of PVSRIPO could be a significant new treatment option (Toyoda et al., 2007).

Currently, several studies using mice suggested that PVSRIPO is an effective treatment methodology. In one study, subcutaneous implantation of neuroblastoma followed by direct tumoral administration of attenuated poliovirus resulted in complete eradication of the tumor. Immunological analyses indicated that this tumor was eliminated, in part, by CD8(+) T cells (Toyoda et al., 2011). In another study, twelve athymic mice were implanted with glioma xenographs in vivo. After a period of time to allow for tumor growth, PVSRIPO inoculation was administered. Ten days after PVSRIPO inoculation, the median tumor size had shrunk by approximately 45%. After another 18 days, tumors were destroyed in these mice indicating that even in the absence of T cells, the PVSRIPO is effective in eliminating tumor cells (Dobrikova et al., 2008). Phase I clinical trials for treatment of human glioblastoma by PVSRIPO are currently in progress with continued patient recruitment at Duke University (Gromeier et al., 2014). In this clinical trial, upon biopsy confirmation of a viable tumor, a catheter is implanted into the tumor that directly delivers the PVSRIPO suspension to the glioblastoma. The catheter is then removed immediately after inoculation and the patients are radiographically evaluated after treatment for tumor changes (Friedman, 2000). PVSRIPO induces a lethal and irreversible virolytic effect and host immune response cytotoxic to the tumor as early as one hour post administration and favorable outcomes have thus far been recorded as many as 20 months after treatment (Gromeier et al., 2014). Should the results of this trial remain positive, further clinical trials using PVSRIPO to treat other types of cancer are warranted.

Risks and Benefits of Oncolytic Virotherapy

Oncolytic virotherapy as a treatment is in its infancy. Therefore, factors regarding the overall safety and optimization of this therapy have not yet been fully vetted. Relative to the current standard of care, virotherapy is much less invasive and debilitating (Fong, 2015). Moreover, this form of oncolytic therapy is highly selective. Injections can be administered locally, which ensure an increased uptake by tumor cells. The viral machinery has been engineered to allow for selection and replication within tumor cells, limiting infection of non-cancer cells of the patient. The poliovirus itself has added benefits (Fong, 2015). The poliovirus has a large RNA size capability making this virus amenable to genetic manipulations. Virotherapies such as PVSRIPO have the ability to specifically target cancer cells and efficiently induce lysis (David et al., 2009). However, this efficiency necessitates the development of patient selection criteria. Currently, there is no standard dose for virotherapy as certain viruses and tumors require different dosage paradigms (David et al., 2009). Ultimately, a dosing strategy will be created that maximizes effectiveness and minimizes risk (Fong, 2015). The optimization of viral production will also be a challenge; little information about cost is currently available. Hospitals will also face challenges with administration, transport, storage and disposal of these viral agents. Although these viruses are attenuated, they pose a potential threat to immuno-compromised patients. Many challenges lie ahead involving the potential implementation of these treatments. However, PVSRIPO serves as a promising treatment option for the future of cancer therapy and may usher in a wave of virus-based therapeutics (Fong, 2015).

Significance

According to the Centers for Disease Control and Prevention (CDC) National Program of Cancer Registries (NPCR) most recent report of national cancer trends, 426.6 of every 100,000 of people who obtained medical attention in 2010 registered as a cancer patient28 These cancers included types such as prostate cancers, lung cancers, leukemia, esophageal and stomach cancers, to breast and lymphatic cancers (Edwards et al., 2014). The number of patients who have cancer in the United states, in addition to the broad spectrum of body systems that cancer can affect, impresses the importance of exploring safe and effective new treatments of all cancers. Additionally, the process of a cell becoming malignant is dynamic and unique, much like the patients who will be receiving treatment. Therefore, treatment should be able to meet the demands of the dynamic process of cancer development without harming the healthy cells within the host.

Cancers arise from an accumulation of genetic mutations that transform a healthy cell into one that causes disease. Because cancer cells are nearly identical to healthy cells, selective toxicity with current standard therapies is difficult to attain. Further, difficulty arises from the inability to determine the specific changes the cancers undergo to create malignancy (Workenhe and Mossman, 2014). Due to the rapid ability of a virus to be changed by recombinant RNA technology, researchers may be able to make “designer viruses” specific to a patient's treatment needs (Parato et al., 2005). Viruses can be modified to invade cancer cells depending on status and speed of growth, receptor type displayed on cancer cell surface, or transcriptional and translational pathway targets within the specific cancer type (Parato et al., 2005). By targeting these specific mechanisms, viruses can potentially be designed to target the unique process that culminate in malignancy. Recombinant genetic technology may allow oncologists to create an oncolytic virus that targets the specific cancer cell type and location. A virus’ propensity to replicate within a host cell and to target cells specifically provides oncolytic virotherapy a pharmacokinetic advantage over conventional cancer therapies (Parato et al., 2005).

As previously mentioned, oncolytic viruses have the ability to stimulate the patient’s immune system while replicating within the tumor cells. Replication within the tumor cells leads to a recruitment of immune cells to this area. In addition to enhancing the cancer fighting ability of the body, this immune activation may benefit patients that have developed immuno-tolerance to their current standard of care chemotherapeutic (Workenhe and Mossman, 2014). Continued use of chemotherapies can lead to cancer cells that are drug resistant or tolerant to these conventional therapies (Workenhe and Mossman, 2014). By using a viral modality to trigger cancer death which involves activation of the host immune response in combination with the use of conventional cancertargeting treatment, drug resistance and tolerance may be limited (Workenhe and Mossman, 2014)

Clinical Perspective

Given the current progress of the experimental and clinical phases of PVSRIPO therapy, the possibility exists that this recombinant virus will soon be a viable treatment option for glioblastoma and various other cancer types. While many healthcare providers and cancer patients may embrace this new virotherapy, history suggests that some may be skeptical and avoid the use because of the viral composition of this treatment. For instance, attenuated viruses have been used safely for decades to vaccinate individuals preventing countless cases of polio, mumps, measles, rubella and other viral diseases. However, due to a fraudulent study and a media explosion, some individuals falsely believe that vaccines cause autism. We suspect that cancer patients and even some physicians may be skeptical of PVSRIPO due to the viral nature of this therapy. Then again, the imminent threat of cancer may offset any fears. Patient education efforts and physician outreach may be necessary to establish virotherapy as a safe cancer treatment option. The very first oncolytic virotherapy has just recently been approved by the FDA (Greig, 2016). This therapytalimogene laherparepvec (Imlygic) can be used to treat patients with skin and lymph node melanoma lesions (Greig, 2016). Talimogene laherparepvec is comprised of an attenuated herpes virus that causes cancer cells to produce GM-CSF, a potent cytokine that acts as a growth factor for white blood cells and induces differentiation of monocytes. Lessons learned from the use of talimogene laherparepvec will undoubtedly contribute to the education efforts and implementation of forthcoming virotherapies such as PVSRIPO.

Based on a cohort study of FDA trends of expedited drug development and approval programs, the novelty and aforementioned advantages of PVSRIPO indicate that this treatment has the potential to be approved for patient use (Kesselheim et al., 2015). Pending FDA approval, physicians will have the option to implement this novel form of therapy for their patients. As with all initiative therapies, the physician needs to play an active role in patient education. The patient should be informed of the mechanism of action of this form of therapy to fully understand the oncolytic role PVSRIPO will play in the treatment of the patient’s cancer. Additionally, all potential adverse reactions should be fully disclosed to all potential patients. Although evidence suggests that PVSRIPO has the potential to provide great therapeutic benefit to cancer patients, we hypothesize that use in clinical practice will rely heavily on physician acceptance and patient education.

Funding Information

This work was supported in part from a grant by an Institutional Development Award (IDeA) from the National Institute of General Medical Sciences of the National Institutes of Health (P20GM103434).

Author’s Contributions

Risk and benefit constructed by Hannah Crewdson and Alexandra Higginbotham. Methods contructed by Hannah Crewdon. The brief history and the premise of Oncolytic Therapy created by Katherine Moio. The normal infectious process of polioviruses constructed by Nicole Rucinsky. Ross Keffer constructed mechanism and therapeutic benefit of PVSRIPO. Diana Remenar and Brianne Clark contributed the sections Current Application. Andrew Stegmen contributed the section Risk and Benefits of Oncolytic Virothereapy. Significance written by Elizabeth Dennistion. Sarah Brammer corresponded with the medical team at Ohio Valley Medical Center, acted as a consult for the clinical application section and edited the manuscript. Joseph Horzempa constructed the abstract, edited and contributed writing to all sections.

Ethics

The authors do not make any recommendation for or against the use of recombinant virotherapy. A physician should be consulted regarding cancer treatment options. The authors declare no conflict of interest.

References

Baskar, R., K.A. Lee, R. Yeo and K.W. Yeoh, 2012. Cancer and radiation therapy: Current advances and future directions. Int. J. Med. Sci., 9: 193-199. DOI: 10.7150/ijms.3635

Brown, M. and M. Gromier, 2015. Oncolytic immunotherapy through tumor-specific translation and cytotoxicity of poliovirus. Discovery Medicine.

Brown, M.C., E.Y. Dobrikova, M.I. Dobrikov, R.W. Walton and S.L. Gemberling et al., 2014. Oncolytic polio virotherapy of cancer. Cancer, 120: 3277-3286. DOI: 10.1002/cncr.28862

Chan, W.M. and G. McFadden, 2014. Oncolytic poxviruses. Ann. Rev. Virol., 1: 119-141. DOI: 10.1146/annurev-virology-031413-085442

Chi, C., Y. Du, J. Ye, D. Kou and J. Qiu et al., 2014. Intraoperative imaging-guided cancer surgery: From current fluorescence molecular imaging methods to future multi-modality imaging technology. Theranostics, 4: 1072-1084. DOI: 10.7150/thno.9899

David, H., K. Thorne and S. Thorne, 2009. Targeted and armed oncolytic poxviruses: A novel multimechanistic therapeutic class for cancer. Nat. Rev. Cancer, 9: 64-71. DOI: 10.1038/nrc2545

Dobrikova, E.Y., T. Broadt, J. Poiley-Nelson, Z. Yang and G. Soman et al., 2008. Recombinant oncolytic poliovirus eliminates glioma in vivo without genetic adaptation to a pathogenic phenotype. Mol. Ther., 16: 1865-1872. DOI: 10.1038/mt.2008.184

Edwards, B.K., A.M. Noone, A.B. Mariotto, E.P. Simard and F.P. Boscoe et al., 2014. Annual report to the nation on the status of cancer, 1975-2010, featuring prevalence of comorbidity and impact on survival among persons with lung, colorectal, breast, or prostate cancer. Cancer, 120: 1290-1314. DOI: 10.1002/cncr.28509

Fong, Y., 2015. Oncolytic treatment for cancer recommended for approval. Mol. Ther., 23: 1131-1131. DOI: 10.1038/mt.2015.94

Friedman, A., 2000. Poliovirus Vaccine for Recurrent Glioblastoma Multiforme (GBM) (PVS-RIPO). In: ClinicalTrials.gov [Internet]. Bethesda (MD): National Library of Medicine (US).

Goetz, C. and M. Gromeier, 2010. Preparing an oncolytic poliovirus recombinant for clinical application against glioblastoma multiforme. Cytokine Growth Factor Rev., 21: 197-203. DOI: 10.1016/j.cytogfr.2010.02.005

Goetz, C., E. Dobrikova, M. Shveygert, M. Dobrikov and M. Gromeier, 2011. Oncolytic poliovirus against malignant glioma. Future Virol., 6: 1045-1058. DOI: 10.2217/fvl.11.76

Goldfarb, M., S. Brower and S.D. Schwaitzberg, 2010. Minimally invasive surgery and cancer: controversies part 1. Surgical Endoscopy, 24: 304-334. DOI: 10.1007/s00464-009-0583-3

Greig, S.L., 2016. Talimogene laherparepvec: First global approval. Drugs, 76: 147-54. DOI: 10.1007/s40265-015-0522-7

Gromeier, M., E. Dobrikova, M. Dobrikov, M. Brown and J. Bryant et al., 2014. Oncolytic poliovirus immunotherapy of glioblastoma. Neuro Oncol., 16: 41-41. DOI: 10.1093/neuonc/nou208.69

Hashiguchi, Y., M. Kasai, T. Fukuda, T. Ichimura and T. Yasui et al., 2015. Chemotherapy-induced neutropenia and febrile neutropenia in patients with gynecologic malignancy. Anti-Cancer Drugs, 26: 1054-1060. DOI: 10.1097/CAD.0000000000000279

Hogle, J.M., 2002. Poliovirus cell entry: Common structural themes in viral cell entry pathways. Annu. Rev. Microbiol., 56: 677-702. DOI: 10.1146/annurev.micro.56.012302.160757

Kesselheim, A.S., B. Wang, J.M. Franklin and J.J. Darrow, 2015. Trends in utilization of FDA expedited drug development and approval programs, 1987-2014: Cohort study. British Med. J., 351: h4633-h4633. DOI: 10.1136/bmj.h4633

Kotla, S. and K.E. Gustin, 2015. Proteolysis of MDA5 and IPS-1 is not required for inhibition of the type I IFN response by poliovirus. Virol. J., 12: 158-158. DOI: 10.1186/s12985-015-0393-2

Larson, C., B. Oronsky, J. Scicinski, G.R. Fanger and M. Stirn et al., 2015. Going viral: A review of replication-selective oncolytic adenoviruses. Oncotarget, 6: 19976-19989. DOI: 10.18632/oncotarget.5116

Merrill, M.K., G. Bernhardt, J.H. Sampson, C.J. Wikstrand and D.D. Bigner et al., 2004. Poliovirus receptor CD155-targeted oncolysis of glioma. NeuroOncology, 6: 208-217. DOI: 10.1215/S1152851703000577

Parato, K.A., D. Senger, P.A. Forsyth and J.C. Bell, 2005. Recent progress in the battle between oncolytic viruses and tumours. Nat. Rev. Cancer, 5: 965-976. DOI: 10.1038/nrc1750

Rapoport, B.L., A. Molasiotis, H. Raftopoulos and F. Roila, 2015. Chemotherapy-induced nausea and vomiting. BioMed Res. Int., 2015: 457326-457327. DOI: 10.1155/2015/457326

Reyes-Gibby, C.C., J. Wang, S.C.J. Yeung and S. Shete, 2015. Informative gene network for chemotherapyinduced peripheral neuropathy. BioData Min., 8: 24-24. DOI: 10.1186/s13040-015-0058-0

Siegel, R., C. DeSantis, K. Virgo, K. Stein and A. Mariotto et al., 2012. Cancer treatment and survivorship statistics, 2012. CA Cancer J. Clin., 62: 220-241. DOI: 10.3322/caac.21149

Southam, C.M., 1960. Division of microbiology: Present status of oncolytic virus studies. Trans. N.Y. Acad. Sci., 22: 657-673. DOI: 10.1111/j.2164-0947.1960.tb00739.x

Stubbe, C.E. and M. Valero, 2013. Complementary strategies for the management of radiation therapy side effects. J. Adv. Practitioner Oncol., 4: 219-231. PMID: 25032003

Sugerman, D., 2013. Chemotherapy. JAMA, 310: 218-218. DOI: 10.1001/jama.2013.5525

Sze, D.Y., T.R. Reid and S.C. Rose, 2013. Oncolytic virotherapy. J. Vascular Intervent. Radiol., 24: 1115-1122. DOI: 10.1016/j.jvir.2013.05.040

Toyoda, H., E. Wimmer and J. Cello, 2011. Oncolytic poliovirus therapy and immunization with poliovirus-infected cell lysate induces potent antitumor immunity against neuroblastoma in vivo. Int. J. Oncol., 38: 81-87. PMID: 21109928

Toyoda, H., J. Yin, S. Mueller, E. Wimmer and J. Cello, 2007. Oncolytic treatment and cure of neuroblastoma by a novel attenuated poliovirus in a novel poliovirus-susceptible animal model. Cancer Res., 67: 2857-64. DOI: 10.1158/0008-5472.CAN-06-3713

Workenhe, S.T. and K.L. Mossman, 2014. Oncolytic` virotherapy and immunogenic cancer cell death: Sharpening the sword for improved cancer treatment strategies. Mol. Ther., 22: 251-256. DOI: 10.1038/mt.2013.220