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76-494: The potential use of echovirus as an oncolytic virus to treat cancer was discovered by Latvian scientist and immunologist Aina Muceniece in the 1960s and 1970s. The virus was obtained from intestinal tract of a healthy children and has not been genetically modified. She was an honorary member of the Latvian Association of Oncologists and the founder of The Aina Muceniece Virotherapy Foundation . The data used to register

152-554: A polymer such as polyethylene glycol , shielding it from antibodies, but this also prevents viral coat proteins adhering to host cells. Another way to help oncolytic viruses reach cancer growths after intravenous injection, is to hide them inside macrophages (a type of white blood cell ). Macrophages automatically migrate to areas of tissue destruction, especially where oxygen levels are low, characteristic of cancer growths, and have been used successfully to deliver oncolytic viruses to prostate cancer in animals. Although it poses

228-399: A "bystander effect" on surrounding tumour cells has been described with several suicide gene systems. Angiogenesis (blood vessel formation) is an essential part of the formation of large tumour masses. Angiogenesis can be inhibited by the expression of several genes, which can be delivered to cancer cells in viral vectors , resulting in suppression of angiogenesis, and oxygen starvation in

304-472: A 5' cap. Gromeier et al. (2000) replaced the normal poliovirus IRES with a rhinovirus IRES, altering tissue specificity. The resulting PV1(RIPO) virus was able to selectively destroy malignant glioma cells, while leaving normal neuronal cells untouched. Reoviruses generally infect mammalian respiratory and bowel systems (the name deriving from an acronym, respiratory enteric orphan virus). Most people have been exposed to reovirus by adulthood; however,

380-479: A criminal offence has occurred. According to Olsena, police has the duty to protect people; it is a dangerous precedent when people receive medicines that do not contain the substance which should be present. A member of Latvian parliament and advisor to the Prime Minister, Renars Putnins , also has called the entire thing an affair and has asked for an official investigation. In Latvia manufacturers of ECHO-7 have

456-496: A history of receiving fines for off-label marketing this anti-cancer drug directly to general public and cancer patients. However, on October 31, 2018 the Regional Administrative Court of Latvia canceled the sanction imposed by the local Health Inspectorate for the unauthorized off-label advertising. Oncolytic virus An oncolytic virus is a virus that preferentially infects and kills cancer cells . As

532-468: A hurdle by inactivating viruses, the patient's immune system can also act as an ally against tumors; infection attracts the attention of the immune system to the tumour and may help to generate useful and long-lasting antitumor immunity. One important mechanism is the release of substances by tumor lysis, such as tumor-associated antigens and danger associated-molecular patterns (DAMPs), which can elicit an antitumor immune response. This essentially produces

608-432: A major cause of mortality, there is still a need for novel cancer therapies, garnering this once-sidelined therapy renewed interest. In one case report published in 2024, a scientist Beata Halassy treated her own stage 3 breast cancer using an Edmonston-Zagreb measles vaccine strain (MeV) and then a vesicular stomatitis virus Indiana strain (VSV), both prepared in her own laboratory, in combination with trastuzumab . While

684-518: A marker in cancer diagnostics and staging . Cancer cells are created when the genes responsible for regulating cell division are damaged. Carcinogenesis is caused by mutation and epimutation of the genetic material of normal cells, which upsets the normal balance between proliferation and cell death. This results in uncontrolled cell division in the body. The uncontrolled and often rapid proliferation of cells can lead to benign or malignant tumours (cancer). Benign tumors do not spread to other parts of

760-739: A much smaller amount than claimed by the manufacturer. According to agency's lab director, "It's like buying what you think is lemon juice, but finding that what you have is lemon-flavored water". In March 2019, the distribution of ECHO-7 in Latvia has been stopped. ECHO-7 has also been removed from the list of state-reimbursed medications. On May 31, 2019, the registration licence of ECHO-7 was suspended in Latvia. According to Baltic News Network , "State Agency for Medicines (SAM) has decided to halts registration of Rigvir medication, until all problems have been resolved". It also reported "more than 30 patients, five healthcare institutions and 16 oncologists have turned to

836-481: A personalised cancer vaccine . Many cases of spontaneous remission of cancer have been recorded. Though the cause is not fully understood, they are thought likely to be a result of a sudden immune response or infection. Efforts to induce this phenomenon have used cancer vaccines (derived from cancer cells or selected cancer antigens ), or direct treatment with immune-stimulating factors on skin cancers. Some oncolytic viruses are very immunogenic and may by infection of

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912-455: A potent cytotoxin , which can diffuse to and kill neighbouring cells. One herpes simplex virus, encoding a thymidine kinase suicide gene, has progressed to phase III clinical trials. The herpes simplex virus thymidine kinase phosphorylates the pro-drug , ganciclovir, which is then incorporated into DNA , blocking DNA synthesis. The tumour selectivity of oncolytic viruses ensures that the suicide genes are only expressed in cancer cells, however

988-518: A request to the Ministry of Health of Latvia, State Agency of Medicines, and National Health Service requesting the removal of ECHO-7 from the Register of Medicines of Latvia and from the list of state-compensated medicines. A revision of clinical treatment guidelines for melanoma was also requested. The request was based on the analysis of available research and suggests that there is no conclusive evidence for

1064-399: A role. Stem cell research suggests that excess SP2 protein may turn stem cells into cancer cells. However, a lack of particular co-stimulated molecules that aid in the way antigens react with lymphocytes can impair the natural killer cells' function, ultimately leading to cancer. When a cell is deficient in the capacity to repair DNA damages , such damages tend to be retained within

1140-441: A simple means of identifying cells infected by the experimental virus. This can be done by equipping the virus with " reporter genes " not normally present in viral genomes, which encode easily identifiable protein markers. One example of such proteins is GFP ( green fluorescent protein ) which, when present in infected cells, will cause a fluorescent green light to be emitted when stimulated by blue light. An advantage of this method

1216-431: A synergistic increase in cell death, as well as a significant increase in viral burst size (the number of virus particles released from each cell lysis). No alteration in viral specificity was observed. SEPREHVIR (HSV-1716) has also shown synergy in pre-clinical research when used in combination with several cancer chemotherapies. The anti- angiogenesis drug bevacizumab (anti- VEGF antibody) has been shown to reduce

1292-509: A tissue culture contaminate at Genetic Therapy, Inc. The initial isolate, SVV-001, is being developed as an anti-cancer therapeutic by Neotropix, Inc. under the name NTX-010 for cancers with neuroendocrine features including small cell lung cancer and a variety of pediatric solid tumours. RIGVIR is a drug that was approved by the State Agency of Medicines of the Republic of Latvia in 2004. It

1368-424: A tumour site, where it replicates and induces disease regression, often leading to durable cures. Attenuation of the virus by engineering a deletion of Met-51 of the matrix protein ablates virtually all infection of normal tissues, while replication in tumour cells is unaffected. Recent research has shown that this virus has the potential to cure brain tumours , thanks to its oncolytic properties. Poliovirus

1444-444: A tumour, and when any resulting fever is not suppressed. Systemic therapy (such as through infusion through an intravenous line) is desirable for treating metastatic disease. It is now marketed under the brand name Oncorine. With advances in cancer immunotherapy such as immune checkpoint inhibitors , increased attention has been given to using oncolytic viruses to increase antitumor immunity. There are two main considerations of

1520-498: A viral defense mechanism that interacts with a normal human gene p53 , which is very frequently dysregulated in cancer cells. Despite the promises of early in vivo lab work, these viruses do not specifically infect cancer cells, but they still kill cancer cells preferentially. While overall survival rates are not known, short-term response rates are approximately doubled for H101 plus chemotherapy when compared to chemotherapy alone. It appears to work best when injected directly into

1596-422: Is a natural invasive neurotropic virus , making it the obvious choice for selective replication in tumours derived from neuronal cells. Poliovirus has a plus-strand RNA genome, the translation of which depends on a tissue-specific internal ribosome entry site (IRES) within the 5' untranslated region of the viral genome, which is active in cells of neuronal origin and allows translation of the viral genome without

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1672-401: Is a normal process used by the body for growth and repair. A parent cell divides to form two daughter cells, and these daughter cells are used to build new tissue or to replace cells that have died because of aging or damage. Healthy cells stop dividing when there is no longer a need for more daughter cells, but cancer cells continue to produce copies. They are also able to spread from one part of

1748-509: Is a rhabdovirus, consisting of 5 genes encoded by a negative sense, single-stranded RNA genome. In nature, VSV infects insects as well as livestock, where it causes a relatively localized and non-fatal illness. The low pathogenicity of this virus is due in large part to its sensitivity to interferons, a class of proteins that are released into the tissues and bloodstream during infection. These molecules activate genetic anti-viral defence programs that protect cells from infection and prevent spread of

1824-494: Is a virus that naturally infects cells of the central nervous system and causes encephalitis . A genetically engineered form has been pre-clinically tested as an oncolytic virus against the severe brain tumour type glioblastoma . The SFV was genetically modified with microRNA target sequences so that it only replicated in brain tumour cells and not in normal brain cells. The modified virus reduced tumour growth and prolonged survival of mice with brain tumours. The modified virus

1900-436: Is an effective cancer treatment . On 19 March 2019, the manufacturer of ECHO-7, SIA LATIMA, announced the drug's removal from sale in Latvia, quoting financial and strategic reasons and insufficient profitability. However, several days later an investigative TV show revealed that State Agency of Medicines had run laboratory tests on the vials, and found that the amount of ECHO-7 virus is of a much smaller amount than claimed by

1976-422: Is arguably the most successful live biotherapeutic agent because of its critical role in the eradication of smallpox , one of the most deadly diseases in human history. Long before the smallpox eradication campaign was launched, VACV was exploited as a therapeutic agent for the treatment of cancer. In 1922, Levaditi and Nicolau reported that VACV was able to inhibit the growth of various tumors in mice and rats. This

2052-501: Is frequently called Sendai virus in scientific literature, has shown some oncolytic properties that are described in the section Murine respirovirus as an oncolytic agent . An innovative approach of drug development termed " directed evolution " involves the creation of new viral variants or serotypes specifically directed against tumour cells via rounds of directed selection using large populations of randomly generated recombinant precursor viruses. The increased biodiversity produced by

2128-461: Is in conjunction with conventional cancer therapies that oncolytic viruses have often showed the most promise, since combined therapies operate synergistically with no apparent negative effects. Onyx-015 ( dl 1520) underwent trials in conjunction with chemotherapy before it was abandoned in the early 2000s. The combined treatment gave a greater response than either treatment alone, but the results were not entirely conclusive. Vaccinia virus GL-ONC1

2204-466: Is that it can be used on live cells and in patients with superficial infected lesions, it enables rapid non-invasive confirmation of viral infection. Another example of a visual marker useful in living cells is luciferase , an enzyme from the firefly which in the presence of luciferin , emits light detectable by specialized cameras. The E. coli enzymes beta-glucuronidase and beta-galactosidase can also be encoded by some viruses. These enzymes, in

2280-534: The cell cycle . A viral gene whose function is to alter a pathway is dispensable in cells where the pathway is defective, but not in cells where the pathway is active. The enzymes thymidine kinase and ribonucleotide reductase in cells are responsible for DNA synthesis and are only expressed in cells which are actively replicating. These enzymes also exist in the genomes of certain viruses (E.g. HSV, vaccinia) and allow viral replication in quiescent (non-replicating) cells, so if they are inactivated by mutation

2356-399: The complement system can enhance oncolytic virus therapy. Pre-existing immunity can be partly avoided by using viruses that are not common human pathogens. However, this does not avoid subsequent antibody generation. Yet, some studies have shown that pre-immunity to oncolytic viruses doesn't cause a significant reduction in efficacy. Alternatively, the viral vector can be coated with

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2432-512: The senecavirus , resulting in clinical trials . The first oncolytic virus to be approved by a national regulatory agency was genetically unmodified ECHO-7 strain enterovirus RIGVIR , which was approved in Latvia in 2004 for the treatment of skin melanoma ; the approval was withdrawn in 2019. An oncolytic adenovirus , a genetically modified adenovirus named H101 , was approved in China in 2005 for

2508-463: The telomeres of most cells shorten after each division, eventually causing the cell to die, telomerase extends the cell's telomeres. This is a major reason that cancer cells can accumulate over time, creating tumors. In February 2019, medical scientists announced that iridium attached to albumin , creating a photosensitized molecule , can penetrate cancer cells and, after being irradiated with light (a process called photodynamic therapy ), destroy

2584-526: The DNA repair enzyme O-6-methylguanine-DNA methyltransferase is observed in several different kinds of cancer (see Misplaced Pages article O-6-methylguanine-DNA methyltransferase ). Although a DNA repair deficiency can predispose a cell lineage to develop cancer, increased (rather than decreased) expression of a repair capability may also emerge in the progression of cancer cell lineages, and this capability may be clinically important as reviewed by Lingg et al. For instance,

2660-407: The DNA repair gene DMC1 encodes a protein that is normally expressed only in cells undergoing meiosis where it helps maintain an undamaged germ-line . However, DMC1 is also expressed in various cancer cell lines including cervical, breast, and lymphoma cancer cell lines. Expression of meiotic DNA repair genes such as DMC1 may promote tumor cell growth by dealing with endogenous DNA damage within

2736-489: The FDA for advanced melanoma is Amgen's talimogene laherparepvec . The first oncolytic virus to be approved by a regulatory agency was a genetically modified adenovirus named H101 by Shanghai Sunway Biotech. It gained regulatory approval in 2005 from China's State Food and Drug Administration (SFDA) for the treatment of head and neck cancer. Sunway's H101 and the very similar Onyx-15 ( dl 1520) have been engineered to remove

2812-516: The Health Inspectorate with a request to permit them to continue therapy using Rigvir. In response to requests, HI permitted distribution of a single type of Rigvir medication for patients, who are already undergoing melanoma treatment". According to Solvita Olsena, expert in patient safety at the University of Latvia, people who have used ECHO-7 should contact the police, as facts indicate that

2888-512: The ICP34.5 gene, and as a result is no longer able to replicate in terminally differentiated and non- dividing cells but will infect and cause lysis very efficiently in cancer cells, and this has proved to be an effective tumour-targeting strategy. In a wide range of in vivo cancer models, the HSV1716 virus has induced tumour regression and increased survival times. In 1996, the first approval

2964-570: The RIGVIR story that strongly suggest that RIGVIR is probably cancer quackery" citing the "mysterious creator" aspect, the misleading description of the product as "natural" and the use of testimonials to market it. In February 2017, the Association of Oncologists, Association of Chemotherapists, Association of Rare Diseases of Latvia, and the Head of Pharmacology Department of Riga Stradiņš University submitted

3040-399: The Register of Medicines of Latvia. On March 19, 2019, the manufacturer of ECHO-7, SIA LATIMA, announced the drug's removal from sale in Latvia, quoting financial and strategic reasons and insufficient profitability. However, several days later an investigative TV show revealed that State Agency of Medicines had run laboratory tests on the vials, and found that the amount of ECHO-7 virus is of

3116-640: The beginning of the 20th century. Efforts to treat cancer through immunisation or virotherapy (deliberate infection with a virus), began in the mid-20th century. As the technology to create a custom virus did not exist, all early efforts focused on finding natural oncolytic viruses. During the 1960s, promising research involved using poliovirus , adenovirus , Coxsackie virus , ECHO enterovirus RIGVIR , and others. The early complications were occasional cases of uncontrolled infection (resulting in significant morbidity and mortality); an immune response would also frequently develop. While not directly harmful to

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3192-716: The body or invade other tissues. Malignant tumors can invade other organs, spread to distant locations ( metastasis ) and become life-threatening. More than one mutation is necessary for carcinogenesis. In fact, a series of several mutations to certain classes of genes is usually required before a normal cell will transform into a cancer cell. Damage to DNA can be caused by exposure to radiation, chemicals, and other environmental sources, but mutations also accumulate naturally over time through uncorrected errors in DNA transcription , making age another risk factor. Oncoviruses can cause certain types of cancer, and genetics are also known to play

3268-409: The body to another in a process known as metastasis . There are different categories of cancer cell, defined according to the cell type from which they originate. Cancer cells have distinguishing histological features visible under the microscope. The nucleus is often large and irregular, and the cytoplasm may also display abnormalities. The shape, size, protein composition, and texture of

3344-435: The cell at an increased level. These damages, upon replication of the cell’s DNA, may cause replication errors, including mutations that lead to cancer. Numerous inherited DNA repair disorders have been described that increase cancer risk (see Misplaced Pages article DNA repair-deficiency disorder ). In addition, particular DNA repair enzymes have been found to be deficient in multiple cancers. For example, deficient expression of

3420-412: The condition as blood disease, and named it leukämie in 1847 (later anglicised to leukemia ). In 1857, he was the first to describe a type of tumour called chordoma that originated from the clivus (at the base of the skull ). Cancer cells have unique features that make them "immortal" according to some researchers. The enzyme telomerase is used to extend the cancer cell's life span. While

3496-557: The control viruses (including Ad5, Ad11p and Ad3) and was confirmed to generate approximately two logs more viral progeny on freshly isolated human colon tumour tissue than on matching normal tissue. Attenuation involves deleting viral genes, or gene regions, to eliminate viral functions that are expendable in tumour cells, but not in normal cells, thus making the virus safer and more tumour-specific. Cancer cells and virus-infected cells have similar alterations in their cell signalling pathways, particularly those that govern progression through

3572-438: The desired therapeutic characteristics. Directed evolution was applied on human adenovirus , one of many viruses that are being developed as oncolytic agents, to create a highly selective and yet potent oncolytic vaccine. As a result of this process, ColoAd1 (a novel chimeric member of the group B adenoviruses) was generated. This hybrid of adenovirus serotypes Ad11p and Ad3 shows much higher potency and tumour selectivity than

3648-476: The drug in Latvia is not sufficient to obtain approval to use it in the US, Europe, or Japan. As of 2017 there was no good evidence that ECHO-7 is an effective cancer treatment . Oncologists and other medical experts in Latvia have repeatedly expressed the concern for the lack of clinical trials and evidence of efficacy, as well as unethical advertising. Oncologist David Gorski has written that "There are many aspects to

3724-464: The efficacy of RIGVIR as a cancer treatment. In 2017 the Health Ministry of Latvia responded that RIGVIR would remain on its medicines register, and that in its judgement the risk-benefit ratio for RIGVIR as acceptable. At the end of 2018, Commission of Social and Labor Affairs of Latvian Parliament started a discussion about possible exclusion of RIGVIR from the list of state-compensated medicines and

3800-457: The infected cancer cells are destroyed by oncolysis , they release new infectious virus particles or virions to help destroy the remaining tumour. Oncolytic viruses are thought not only to cause direct destruction of the tumour cells, but also to stimulate host anti-tumour immune system responses. Oncolytic viruses also have the ability to affect the tumor micro-environment in multiple ways. The potential of viruses as anti-cancer agents

3876-445: The infection does not typically produce symptoms. The reovirus' oncolytic potential was established after they were discovered to reproduce well in various cancer cell lines, lysing these cells. Reolysin is a formulation of reovirus intended to treat various cancers currently undergoing clinical trials. Senecavirus , also known as Seneca Valley Virus, is a naturally occurring wild-type oncolytic picornavirus discovered in 2001 as

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3952-533: The inflammatory response to oncolytic HSV and improve virotherapy in mice. A modified oncolytic vaccinia virus encoding a single-chain anti-VEGF antibody (mimicking bevacizumab) was shown to have significantly enhanced antitumor activities than parental virus in animal models. In science fiction, the concept of an oncolytic virus was first introduced to the public in Jack Williamson 's novel Dragon's Island , published in 1951, although Williamson's imaginary virus

4028-480: The initial homologous recombination step provides a large random pool of viral candidates which can then be passed through a series of selection steps designed to lead towards a pre-specified outcome (e.g. higher tumor specific activity) without requiring any previous knowledge of the resultant viral mechanisms that are responsible for that outcome. The pool of resultant oncolytic viruses can then be further screened in pre-clinical models to select an oncolytic virus with

4104-440: The interaction between oncolytic viruses and the immune system. A major obstacle to the success of oncolytic viruses is the patient immune system which naturally attempts to deactivate any virus. This can be a particular problem for intravenous injection, where the virus must first survive interactions with the blood complement and neutralising antibodies. It has been shown that immunosuppression by chemotherapy and inhibition of

4180-422: The manufacturer. According to agency's lab director, "It's like buying what you think is lemon juice, but finding that what you have is lemon-flavored water". In March 2019, the distribution of ECHO-7 in Latvia has been stopped. Based on the request of some patients, medical institutions and physicians were allowed to continue use despite the suspension of the registration certificate. Semliki Forest virus (SFV)

4256-441: The nucleus are often altered in malignant cells . The nucleus may acquire grooves, folds or indentations, chromatin may aggregate or disperse, and the nucleolus can become enlarged. In normal cells, the nucleus is often round or solid in shape, but in cancer cells the outline is often irregular. Different combinations of abnormalities are characteristic of different cancer types, to the extent that nuclear appearance can be used as

4332-607: The oldest documented malignant hominin cancer. The understanding of cancer was significantly advanced during the Renaissance period and in to the Age of Discovery . Sir Rudolf Virchow , a German biologist and politician , studied microscopic pathology, and linked his observations to illness. He is described as "the founder of cellular pathology". In 1845, Virchow and John Hughes Bennett independently observed abnormal increase in white blood cells in patients. Virchow correctly identified

4408-596: The outer coating of HSV1716 variants can be targeted to specific types of cancer cells, and can be used to deliver a variety of additional genes into cancer cells, such as genes to split a harmless prodrug inside cancer cells to release toxic chemotherapy, or genes which command infected cancer cells to concentrate protein tagged with radioactive iodine , so that individual cancer cells are killed by micro-dose radiation as well as by virus-induced cell lysis. Other oncolytic viruses based on HSV have also been developed and are in clinical trials. One that has been approved by

4484-546: The patient, the response destroyed the virus thus preventing it from destroying the cancer. Early efforts also found that only certain cancers could be treated through virotherapy . Even when a response was seen, these responses were neither complete nor durable. The field of virotherapy was nearly abandoned for a time, as the technology required to modify viruses didn't exist whereas chemotherapy and radiotherapy technology enjoyed early success. However, now that these technologies have been thoroughly developed and cancer remains

4560-411: The presence of certain substrates, can produce intense colored compounds useful for visualizing infected cells and also for quantifying gene expression. Oncolytic viruses can be used against cancers in ways that are additional to lysis of infected cells. Viruses can be used as vectors for delivery of suicide genes, encoding enzymes that can metabolise a separately administered non-toxic pro-drug into

4636-466: The surface of the cell. These work to help macrophages detect and kill cancer cells. Early evidence of human cancer can be interpreted from Egyptian papers (1538 BCE) and mummified remains. In 2016, a 1.7 million year old osteosarcoma was reported by Edward John Odes (a doctoral student in Anatomical Sciences from Witwatersrand Medical School, South Africa) and colleagues, representing

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4712-1052: The treatment of head and neck cancer. In 2015, talimogene laherparepvec (OncoVex, T-VEC), an oncolytic herpes virus which is a modified herpes simplex virus, became the first oncolytic virus to be approved for use in the United States and the European Union , for the treatment of advanced inoperable melanoma . On 16 December 2022, the Food and Drug Administration approved nadofaragene firadenovec-vncg (Adstiladrin, Ferring Pharmaceuticals) for adult patients with high-risk Bacillus Calmette-Guérin (BCG) unresponsive non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ (CIS) with or without papillary tumors. A connection between cancer regression and viruses has long been theorised, and case reports of regression noted in cervical cancer , Burkitt lymphoma , and Hodgkin lymphoma , after immunisation or infection with an unrelated virus appeared at

4788-566: The treatment was successful and self-experimentation has a long history in science, the decision to publish the case report attracted controversy due to the unapproved nature of the viral agents and treatment protocol used. Herpes simplex virus (HSV) was one of the first viruses to be adapted to attack cancer cells selectively, because it was well understood, easy to manipulate and relatively harmless in its natural state (merely causing cold sores ) so likely to pose fewer risks. The herpes simplex virus type 1 (HSV-1) mutant 1716 lacks both copies of

4864-421: The tumor, and may also diminish the effectiveness of anticancer therapy, such as radiation therapy . Cells playing roles in the immune system, such as T-cells , are thought to use a dual receptor system when they determine whether or not to kill sick or damaged human cells. If a cell is under stress, turning into tumors, or infected, molecules including MIC-A and MIC-B are produced so that they can attach to

4940-432: The tumour, elicit an anti-tumor immune response, especially viruses delivering cytokines or other immune stimulating factors. Viruses selectively infect tumor cells because of their defective anti-viral response. Imlygic , an attenuated herpes simplex virus , has been genetically engineered to replicate preferentially within tumor cells and to generate antigens that elicit an immune response. Vaccinia virus (VACV)

5016-403: The tumour. The infection of cells with viruses containing the genes for angiostatin and endostatin synthesis inhibited tumour growth in mice. Enhanced antitumour activities have been demonstrated in a recombinant vaccinia virus encoding anti-angiogenic therapeutic antibody and with an HSV1716 variant expressing an inhibitor of angiogenesis. Addition of the sodium-iodide symporter (NIS) gene to

5092-428: The viral genome causes infected tumour cells to express NIS and accumulate iodine. When combined with radioiodine therapy it allows local radiotherapy of the tumour, as used to treat thyroid cancer. The radioiodine can also be used to visualise viral replication within the body by the use of a gamma camera . This approach has been used successfully preclinically with adenovirus, measles virus and vaccinia virus. It

5168-409: The virus will only be able to replicate in proliferating cells, such as cancer cells. There are two main approaches for generating tumour selectivity: transductional and non-transductional targeting. Double targeting with both transductional and non-transductional targeting methods is more effective than any one form of targeting alone. Both in the laboratory and in the clinic it is useful to have

5244-543: The virus. However, in 2000, Stojdl, Lichty et al. demonstrated that defects in these pathways render cancer cells unresponsive to the protective effects of interferons and therefore highly sensitive to infection with VSV. Since VSV undergoes a rapid cytolytic replication cycle, infection leads to death of the malignant cell and roughly a 1000-fold amplification of virus within 24h. VSV is therefore highly suitable for therapeutic application, and several groups have gone on to show that systemically administered VSV can be delivered to

5320-472: Was also approved in Georgia and Armenia . It is wild type ECHO-7, a member of echovirus group. The potential use of echovirus as an oncolytic virus to treat cancer was discovered by Latvian scientist Aina Muceniece in the 1960s and 1970s. The data used to register the drug in Latvia is not sufficient to obtain approval to use it in the US, Europe, or Japan. As of 2017 there was no good evidence that RIGVIR

5396-585: Was also found to efficiently kill human glioblastoma tumour cell lines. The maraba virus , first identified in Brazilian sandflies, is being tested clinically. Coxsackievirus A21 is being developed by Viralytics under trade name Cavatak. Coxsackievirus A21 belongs to Enterovirus C species. Influenza A is one of the earliest viruses anecdotally reported to induce cancer regression. This has prompted preclinical development of genetically engineered oncolytic influenza A viruses. Murine Respirovirus , which

5472-505: Was based on a bacteriophage rather than a mammalian virus. Dragon's Island is also known for being the source of the term " genetic engineering ". The plot of the Hollywood film I Am Legend is based on the premise that a worldwide epidemic was caused by a viral cure for cancer. Cancer cell Cancer cells are cells that divide continually, forming solid tumors or flooding the blood or lymph with abnormal cells. Cell division

5548-438: Was first realised in the early twentieth century, although coordinated research efforts did not begin until the 1960s. A number of viruses including adenovirus , reovirus , measles , herpes simplex , Newcastle disease virus , and vaccinia have been clinically tested as oncolytic agents. Most current oncolytic viruses are engineered for tumour selectivity, although there are naturally occurring examples such as reovirus and

5624-557: Was given in Europe for a clinical trial using the oncolytic virus HSV1716. From 1997 to 2003, strain HSV1716 was injected into tumours of patients with glioblastoma multiforme , a highly malignant brain tumour, with no evidence of toxicity or side effects, and some long-term survivors. Other safety trials have used HSV1716 to treat patients with melanoma and squamous-cell carcinoma of head and neck. Since then other studies have shown that

5700-445: Was studied in a trial combined with chemo- and radiotherapy as Standard of Care for patients newly diagnosed with head & neck cancer. Herpes simplex virus, adenovirus, reovirus and murine leukemia virus are also undergoing clinical trials as a part of combination therapies. Chen et al. (2001) used CV706, a prostate-specific adenovirus, in conjunction with radiotherapy on prostate cancer in mice. The combined treatment resulted in

5776-513: Was the first demonstration of viral oncolysis in the laboratory. This virus was subsequently shown to selectively infect and destroy tumor cells with great potency, while sparing normal cells, both in cell cultures and in animal models. Since vaccinia virus has long been recognized as an ideal backbone for vaccines due to its potent antigen presentation capability, this combines well with its natural oncolytic activities as an oncolytic virus for cancer immunotherapy . Vesicular stomatitis virus (VSV)

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