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Experimental cancer treatment

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799:(HIFU) is still in investigatory phases in many places around the world. In China it has CFDA approval and over 180 treatment centres have been established in China, Hong Kong, and Korea. HIFU has been successfully used to treat cancer to destroy tumours of the bone, brain, breast, liver, pancreas, rectum, kidney, testes, and prostate. Several thousand patients have been treated with various types of tumours. HIFU has CE approval for palliative care for bone metastasis. Experimentally, palliative care has been provided for cases of advanced pancreatic cancer. High-energy therapeutic ultrasound could increase higher-density anti-cancer drug load and nanomedicines to target tumor sites by 20x fold higher than traditional target cancer therapy. 735:, including gold-coated nanoshells and nanorods that exhibit certain degrees of 'tunability' of the absorption properties of the nanoparticles to the wavelength of light for irradiation. The success of this approach to cancer treatment rests on the existence of an 'optical window' in which biological tissue (i.e., healthy cells) are completely transparent at the wavelength of the laser light, while nanoparticles are highly absorbing at the same wavelength. Such a 'window' exists in the so-called near-infrared region of the electromagnetic spectrum. In this way, the laser light can pass through the system without harming healthy tissue, and only diseased cells, where the nanoparticles reside, get hot and are killed. 708:. The purpose of overheating the tumor cells is to create a lack of oxygen so that the heated cells become overacidified, which leads to a lack of nutrients in the tumor. This in turn disrupts the metabolism of the cells so that cell death (apoptosis) can set in. In certain cases chemotherapy or radiation that has previously not had any effect can be made effective. Hyperthermia alters the cell walls by means of so-called heat shock proteins. The cancer cells then react very much more effectively to the cytostatics and radiation. If hyperthermia is used conscientiously it has no serious side effects. 241:. The dose given in these trials may be far too small to produce any useful effect. In most research, these early trials may involve healthy people, but cancer studies normally enroll only people with relatively severe forms of the disease in this stage of testing. On average, 95% of the participants in these early trials receive no benefit, but all are exposed to the risk of adverse effects. Most participants show signs of 3473: 35: 288:, to consume the interior of oxygen-poor tumours. These should then die when they come in contact with the tumor's oxygenated sides, meaning they would be harmless to the rest of the body. A major problem has been that bacteria do not consume all parts of the malignant tissue. However, combining the therapy with chemotherapeutic treatments can help to solve this problem. 593:, or could enhance the effects of these current treatments. It has been shown that the epigenetic control of the proto-onco regions and the tumor suppressor sequences by conformational changes in histones directly affects the formation and progression of cancer. Epigenetics also has the factor of reversibility, a characteristic that other cancer treatments do not offer. 127: 731:, and direct application of heat through the use of heated saline pumped through catheters. Experiments with carbon nanotubes that selectively bind to cancer cells have been performed. Lasers are then used that pass harmlessly through the body, but heat the nanotubes, causing the death of the cancer cells. Similar results have also been achieved with other types of 749:, as well as of developing new types of nanoparticles that make them particularly efficient absorbers while offering little or no concerns about toxicity to the circulation system. Clinicians also hope to use advanced imaging techniques to monitor heat treatments in real time—heat-induced changes in 544:
destruction of noncancerous cells infected with the vector. However, new studies focus on adenoviruses that can be permitted to reproduce, and destroy cancerous cells in the process, since the adenoviruses' ability to infect normal cells is substantially impaired, potentially resulting in a far more
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Cold atmospheric plasma or CAP for short is an emerging modality for the treatment of solid tumors Recently, cold atmospheric plasma (CAP) indicated promising anti-neoplastic effects on several tumors, e.g. melanoma, glioma, and pancreatic cancer cells , and therefore could be an efficient method
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that protects the cell in response to damage and stress. It is analogous to deciding what to do with a damaged car: p53 brings everything to a halt, and then decides whether to fix the cell or, if the cell is beyond repair, to destroy the cell. This protective function of p53 is disabled in most
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through a tumour region using electrodes external to the body. Successful trials have shown the process effectiveness to be greater than chemotherapy and there are no side-effects and only negligible time spent away from normal daily activities. This treatment is still in very early development
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of drugs, devices, and techniques begins in laboratories, either with isolated cells or in small animals, most commonly rats or mice. In other cases, the proposed treatment for cancer is already in use for some other medical condition, in which case more is known about its safety and potential
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One of the challenges in thermal therapy is delivering the appropriate amount of heat to the correct part of the patient's body. A great deal of current research focuses on precisely positioning heat delivery devices (catheters, microwave, and ultrasound applicators, etc.) using ultrasound or
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for their immortality, it has been proposed that a drug that inactivates telomerase might be effective against a broad spectrum of malignancies. At the same time, most healthy tissues in the body express little if any telomerase, and would function normally in its absence. Currently,
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Gannon CJ, Cherukuri P, Yakobson BI, Cognet L, Kanzius JS, Kittrell C, Weisman RB, Pasquali M, Schmidt HK, Smalley RE, Curley SA (December 2007). "Carbon nanotube-enhanced thermal destruction of cancer cells in a noninvasive radiofrequency field".
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The entries listed below vary between theoretical therapies to unproven controversial therapies. Many of these treatments are alleged to help against only specific forms of cancer. It is not a list of treatments widely available at hospitals.
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Nyquist MD, Ang LS, Corella A, Coleman IM, Meers MP, Christiani AJ, Pierce C, Janssens DH, Meade HE, Bose A, Brady L, Howard T, De Sarkar N, Frank SB, Dumpit RF, Dalton JT, Corey E, Plymate SR, Haffner MC, Mostaghel EA, Nelson PS (2021).
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areas of the tumor, the enzyme is expressed solely in the tumor. Thus, a systemically applied prodrug is metabolised to the toxic drug only in the tumor. This has been demonstrated to be effective with the nonpathogenic anaerobe
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As p53 protein levels are usually kept low, one could block its degradation and allow large amounts of p53 to accumulate, thus stimulating p53 activity and its antitumour effects. Drugs that utilize this mechanism include
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are a commonly utilized vector for this purpose. Much research has focused on the use of adenoviruses that cannot reproduce, or reproduce only to a limited extent, within the patient to ensure safety via the avoidance of
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Jagadeesh S, Banerjee PP (November 2006). "Inositol hexaphosphate represses telomerase activity and translocates TERT from the nucleus in mouse and human prostate cancer cells via the deactivation of Akt and PKCalpha".
1561:"Efficacy of enobosarm, a selective androgen receptor (AR) targeting agent, correlates with the degree of AR positivity in advanced AR+/estrogen receptor (ER)+ breast cancer in an international phase 2 clinical study" 1183:
Issaeva N, Bozko P, Enge M, Protopopova M, Verhoef LG, Masucci M, Pramanik A, Selivanova G (December 2004). "Small molecule RITA binds to p53, blocks p53-HDM-2 interaction and activates p53 function in tumors".
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More prolonged moderate heating to temperatures just a few degrees above normal (39.5 °C) can cause more subtle changes. A mild heat treatment combined with other stresses can cause cell death by
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Most complementary and alternative medicines for cancer have not been rigorously studied or tested. Some alternative treatments that have been proven ineffective continue to be marketed and promoted.
473:(AAS) were historically used successfully to treat AR positive breast cancer, but were phased out after the development of anti-estrogen therapies, due to androgenic side effects and concerns about 1048:
Ventura A, Kirsch DG, McLaughlin ME, Tuveson DA, Grimm J, Lintault L, Newman J, Reczek EE, Weissleder R, Jacks T (February 2007). "Restoration of p53 function leads to tumour regression in vivo".
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Palmieri C, Linden HM, Birrell S, Lim E, Schwartzberg LS, Rugo HS, Cobb PW, Jain K, Vogel CL, O'Shaughnessy J, Johnston SR, Getzenberg RH, Barnette KG, Steiner MS, Brufsky A, Overmoyer B (2021).
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whether these treatments are safe and effective treatments. Experimental cancer treatments are normally available only to people who participate in formal research programs, which are called
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Gürtler U, Tontsch-Grunt U, Jarvis M, Zahn SK, Boehmelt G, Quant J, Adolf GR, Solca F (2010). "Effect of BI 811283, a novel inhibitor of Aurora B kinase, on tumor senescence and apoptosis".
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Hallgren O, Aits S, Brest P, Gustafsson L, Mossberg AK, Wullt B, Svanborg C (2008). "Apoptosis and Tumor Cell Death in Response to HAMLET (Human α-Lactalbumin Made Lethal to Tumor Cells)".
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receptors within the cell. Current research has shown that epigenetic pharmaceuticals could be a putative replacement or adjuvant therapy for currently accepted treatment methods such as
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cancer cells, allowing them to multiply without check. Restoration of p53 activity in tumours (where possible) has been shown to inhibit tumour growth and can even shrink the tumour.
264:. In some cases, the Phase III trial provides the best available treatment to all participants, in addition to some of the patients receiving the experimental treatment. 45: 2398:
Weiss M, Gümbel D, Hanschmann EM, Mandelkow R, Gelbrich N, Zimmermann U, Walther R, Ekkernkamp A, Sckell A, Kramer A, Burchardt M, Lillig CH, Stope MB (1 July 2015).
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Iglesias-Linares A, Yañez-Vico RM, González-Moles MA (May 2010). "Potential role of HDAC inhibitors in cancer therapy: insights into oral squamous cell carcinoma".
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Heydari M, Javidi M, Attar MM, Karimi A, Navidbakhsh M, Haghpanahi M, Amanpour S (2015). "Magnetic Fluid Hyperthermia in a Cylindrical Gel Contains Water Flow".
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is the study of heritable changes in gene activity that are not caused by changes in the DNA sequence, often a result of environmental or dietary damage to the
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to estrogen. SARMs have some of the same therapeutic effects as AAS, but fewer side effects, and they cannot be aromatized. Although a trial on AR positive
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is a novel FDA-approved cancer treatment therapy that uses alternating electric field to disturb the rapid cell division exhibited by cancer cells.
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are the most likely candidate. Promising preclinical trials have been conducted, although clinical trials may not be held for another few years.
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Localized and whole-body application of heat has been proposed as a technique for the treatment of malignant tumours. Intense heating will cause
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makes use of magnetic nanoparticles, which can be injected into tumours and then generate heat when subjected to an alternating magnetic field.
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have a hard time penetrating tumors to kill them at their core because these cells may lack a good blood supply. Researchers have been using
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for anti-cancer treatment in clinical urology in the future. One example of an experimental technology utilizing Cold Atmospheric plasma is
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studies. Early clinical trials typically enroll a very small number of patients, and the purpose is to identify major safety issues and the
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Babington P, Rajjoub K, Canady J, Siu A, Keidar M, Sherman JH (June 2015). "Use of cold atmospheric plasma in the treatment of cancer".
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Hedström E, Issaeva N, Enge M, Selivanova G (February 2009). "Tumor-specific induction of apoptosis by a p53-reactivating compound".
600:, PhD, of Duke University Medical Center, think epigenetics may ultimately turn out to have a greater role in disease than genetics. 85: 1739:
Kanerva A, Lavilla-Alonso S, Raki M, Kangasniemi L, Bauerschmitz GJ, Takayama K, Ristimäki A, Desmond RA, Hemminki A (August 2008).
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studies, enroll more people, and the goal is to determine whether the treatment actually works. Phase III studies are frequently
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Medical research for cancer begins much like research for any disease. In organized studies of new treatments for cancer, the
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or magnetic fluid hyperthermia method, it will be easier to control temperature distribution by controlling the velocity of
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Brown CJ, Lain S, Verma CS, Fersht AR, Lane DP (December 2009). "Awakening guardian angels: drugging the p53 pathway".
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Another strategy is to use anaerobic bacteria that have been transformed with an enzyme that can convert a non-toxic
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Dr med Peter Wolf, 2008, Innovations in biological cancer therapy, a guide for patients and their relatives, p 31-32
380:. As of 2009, there are also other drugs that are still in the preclinical stage of testing, such as RITA and MITA. 3448: 3384: 3036: 746: 441:. Recent research works suggest itraconazole (ITZ) could also be used in the treatment of cancer by inhibiting the 3431: 3391: 2830: 1920: 53: 2257: 3126: 2865: 2823: 217: 1091:
Xue W, Zender L, Miething C, Dickins RA, Hernando E, Krizhanovsky V, Cordon-Cardo C, Lowe SW (February 2007).
1800:"Prostate cancer chemopreventive activity of phenethyl isothiocyanate through epigenetic regulation (review)" 711:
There are many techniques by which heat may be delivered. Some of the most common involve the use of focused
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Mo S, Coussios CC, Seymour L, Carlisle R (December 2012). "Ultrasound-enhanced drug delivery for cancer".
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Heat treatment involves using radio waves to heat up tiny metals that are implanted in cancerous tissue.
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into these cells that make them susceptible to particular chemotherapy agents; studies with introducing
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breast cancer in a phase II study. In patients with more than 40 percent AR positivity as determined by
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Davies AM, Weinberg U, Palti Y (July 2013). "Tumor treating fields: a new frontier in cancer therapy".
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refers to compounds used instead of conventional medicine. CAM use is common among people with cancer.
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Mo S, Carlisle R, Laga R, Myers R, Graham S, Cawood R, Ulbrich K, Seymour L, Coussios CC (July 2015).
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HAMLET (human alpha-lactalbumin made lethal to tumor cells) is a molecular complex derived from human
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are the study of treatments in humans. The first-in-human tests of a potential treatment are called
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Javidi M, Heydari M, Attar MM, Haghpanahi M, Karimi A, Navidbakhsh M, Amanpour S (February 2015).
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is currently conducting two clinical trials involving telomerase inhibitors. One uses a vaccine (
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was ended early due to lack of efficacy, ostarine showed benefits in some patients with ER+, AR+
279: 2658: 2324:"Increasing the density of nanomedicines improves their ultrasound-mediated delivery to tumours" 3280: 3268: 3246: 3229: 3051: 3041: 2953: 2767: 2630: 2585: 2531: 2482: 2439: 2380: 2345: 2296: 2231: 2162: 2071: 2022: 1960: 1897: 1856: 1821: 1780: 1721: 1672: 1654: 1580: 1541: 1492: 1474: 1433: 1379: 1330: 1312: 1244: 1201: 1157: 1122: 1065: 1030: 989: 979: 946: 923: 874: 774: 750: 724: 705: 633: 586: 502: 466: 462: 438: 300: 284: 175:. Occasionally, a seriously ill person may be able to access an experimental drug through an 158: 641: 637: 3421: 3337: 3165: 3143: 2940: 2818: 2622: 2577: 2521: 2474: 2429: 2419: 2372: 2335: 2288: 2223: 2154: 2100: 2061: 2012: 1952: 1887: 1848: 1811: 1770: 1760: 1711: 1703: 1662: 1646: 1607:"FDA Grants Fast Track Designation to Enobosarm in AR+, ER+, HER2- Metastatic Breast Cancer" 1572: 1531: 1523: 1482: 1464: 1423: 1415: 1369: 1361: 1320: 1302: 1271: 1236: 1193: 1149: 1112: 1104: 1093:"Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas" 1057: 1020: 971: 913: 905: 553: 498: 442: 407: 395: 184: 166: 1403: 3290: 3192: 3153: 3056: 3031: 2676: 2668: 2214:
Pless M, Weinberg U (August 2011). "Tumor treating fields: concept, evidence and future".
1741:"Systemic therapy for cervical cancer with potentially regulatable oncolytic adenoviruses" 816: 778: 526: 399: 377: 176: 209:
The twin goals of research are to determine whether the treatment actually works (called
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Javidi M, Heydari M, Karimi A, Haghpanahi M, Navidbakhsh M, Razmkon A (December 2014).
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usually refers to methods and substances used along with conventional medicine, while
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within the cell, including slowed cell division and increased sensitivity to ionizing
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has already reached clinical trial stage in many countries. The concept applies an
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into rapidly dividing cells has been thought to slow down or arrest tumor growth.
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Solomon ZJ, Mirabal JR, Mazur DJ, Kohn TP, Lipshultz LI, Pastuszak AW (2019).
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breast cancer. SARMs have also shown antitumor effects in prostate cancer.
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Vickers A (2004). "Alternative cancer cures: "unproven" or "disproven"?".
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Christiansen AR, Lipshultz LI, Hotaling JM, Pastuszak AW (March 2020).
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if you can. Unsourced or poorly sourced material may be challenged and
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that kills tumor cells by a process resembling programmed cell death (
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programs normally refuse to pay for experimental cancer treatments.
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by improving on, supplementing or replacing conventional methods (
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Boohaker RJ, Lee MW, Vishnubhotla P, Perez JL, Khaled AR (2012).
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Because most malignant cells rely on the activity of the protein
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into a toxic drug. With the proliferation of the bacteria in the
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are sometimes perceptible using these imaging instruments. In
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A number of research groups have experimented with the use of
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Another method that is entirely non-invasive referred to as
410:. As of 2010, BI 811283 is currently in the early stages of 668:. The drug is triggered by light of a specific wavelength. 325:
HAMLET (human alpha-lactalbumin made lethal to tumor cells)
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HAMLET (human alpha-lactalbumin made lethal to tumor cells)
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and is undergoing first-in-human trials in patients with
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National Center for Complementary and Integrative Health
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Martins CP, Brown-Swigart L, Evan GI (December 2006).
337:). As of 2008, it had been tested in humans with skin 245:(the irrational belief that they will beat the odds). 943:
Clostridia: Molecular Biology in the Post-genomic Era
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Mengesha (2009). "Clostridia in Anti-tumor Therapy".
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Several drug therapies are being developed based on
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Biochemical and Biophysical Research Communications
1690:Rein DT, Breidenbach M, Curiel DT (February 2006). 548:Another use of gene therapy is the introduction of 640:) and the other uses a lipidated oligonucleotide ( 700:. There are many biochemical consequences to the 3208:Strategies for engineered negligible senescence 2054:Journal of Biomedical Physics & Engineering 1289:Li K, Fang D, Xiong Z, Luo R (23 August 2019). 59:Please review the contents of the article and 3083: 2684: 8: 2189:"The cure to cancer could be in your radio!" 2092:Journal of Mechanics in Medicine and Biology 1874:Li LC, Carroll PR, Dahiya R (January 2005). 3472: 3109: 3090: 3076: 3068: 2719: 2691: 2677: 2669: 2459:Annals of the New York Academy of Sciences 2616: 2525: 2433: 2423: 2339: 2065: 2016: 1891: 1815: 1774: 1764: 1715: 1666: 1535: 1486: 1468: 1427: 1373: 1324: 1306: 1116: 1024: 917: 693:, rapidly killing cells within a tumour. 628:, and as of 2005 and 2006 phase I and II 1880:Journal of the National Cancer Institute 1510:Narayanan R, Coss CC, Dalton JT (2018). 833:Complementary and alternative treatments 2216:Expert Opinion on Investigational Drugs 865: 3328:Differential technological development 1397: 1395: 1393: 844:Complementary and alternative medicine 664:(Tookad, WST09, WST11), Photofrin, or 453:Selective androgen receptor modulators 376:and MI-219, which are both in phase I 179:program. Some of the treatments have 2005:International Journal of Hyperthermia 1987:Hyperthermia - Cancer therapy hots up 1639:The Journal of Clinical Investigation 7: 3134:Aldehyde-stabilized cryopreservation 2191:. Winknews.com. 2007. Archived from 1798:Wang LG, Chiao JW (September 2010). 1516:Molecular and Cellular Endocrinology 3417:Future-oriented technology analysis 2605:CA: A Cancer Journal for Clinicians 2118:David Templeton (18 January 2007). 1457:Translational Andrology and Urology 1276:10.1200/jco.2010.28.15_suppl.e13632 564:, are in their experimental stage. 433:, sometimes abbreviated ITZ, is an 2258:"Tumour Treating Fields explained" 1853:10.1016/j.oraloncology.2010.01.009 25: 1804:International Journal of Oncology 1577:10.1200/JCO.2021.39.15_suppl.1020 873:Chen, Pauline W. (3 March 2011). 803:Cold atmospheric plasma treatment 797:High-intensity focused ultrasound 793:stages for many types of cancer. 769:Noninvasive cancer heat treatment 3471: 183:for treating other conditions. 125: 33: 2659:"Questionable Cancer Therapies" 2281:Expert Opinion on Drug Delivery 604:Telomerase deactivation therapy 469:(ER) positive and AR positive. 75:"Experimental cancer treatment" 3500:Experimental cancer treatments 875:"When Optimism Is Unrealistic" 199:Studying treatments for cancer 139:Experimental cancer treatments 61:add the appropriate references 1: 3444:Technology in science fiction 3006:Clonally transmissible cancer 2508:Cassileth BR, Deng G (2004). 2341:10.1016/j.jconrel.2015.05.265 2328:Journal of Controlled Release 839:Alternative cancer treatments 560:, making them susceptible to 493:(CBR) was 80 percent and the 479:triple negative breast cancer 165:). However, researchers are 2570:Journal of Clinical Oncology 2554:. retrieved 3 February 2008. 2527:10.1634/theoncologist.9-1-80 2425:10.1371/journal.pone.0130350 2293:10.1517/17425247.2012.739603 2228:10.1517/13543784.2011.583236 2018:10.3109/02656736.2014.988661 1766:10.1371/journal.pone.0002917 1565:Journal of Clinical Oncology 968:Bioactive Components of Milk 471:Anabolic androgenic steroids 258:randomized controlled trials 145:therapies intended to treat 2582:10.1200/JCO.2000.18.13.2505 1270:(15 Suppl e13632): e13632. 1241:10.1016/j.yexcr.2008.11.009 976:10.1007/978-0-387-74087-4_8 898:Current Medicinal Chemistry 402:protein being developed by 189:publicly funded health care 46:reliable medical references 3516: 3449:Technology readiness level 3385:Technological unemployment 3037:Index of oncology articles 2564:Richardson MA, Sanders T, 1957:10.1016/j.bbrc.2006.09.002 1402:Dai C, Ellisen LW (2023). 1366:10.1016/j.sxmr.2018.09.006 1229:Experimental Cell Research 1026:10.1016/j.cell.2006.12.007 945:. Caister Academic Press. 910:10.2174/092986712801661004 836: 822:Electromagnetic treatments 747:magnetic resonance imaging 675: 571: 520: 437:used to treat a number of 352: 322: 202: 3467: 3432:Technological singularity 3392:Technological convergence 2627:10.3322/canjclin.54.2.110 2105:10.1142/S0219519415500888 1528:10.1016/j.mce.2017.06.013 596:Some investigators, like 167:still trying to determine 52:or relies too heavily on 3127:Microgravity bioprinting 1708:10.2217/14796694.2.1.137 218:pre-clinical development 3397:Technological evolution 3370:Exploratory engineering 3298:Whole genome sequencing 2959:Prostate cancer staging 2923:Paraneoplastic syndrome 2124:Pittsburgh Post-Gazette 1470:10.21037/tau.2019.11.02 1354:Sexual Medicine Reviews 1295:OncoTargets and Therapy 672:Hyperthermiatic therapy 495:objective response rate 420:Acute Myeloid Leukaemia 18:Gene therapy for cancer 3407:Technology forecasting 3402:Technological paradigm 3375:Proactionary principle 3259:Robot-assisted surgery 2997:Tumor suppressor genes 2964:Gleason grading system 2918:Precancerous condition 1915:Beil L (Winter 2008). 1463:(Suppl 2): S135–S148. 1420:10.1093/oncolo/oyad049 1142:Nature Reviews. Cancer 848:Complementary medicine 815:23 August 2018 at the 763:magnetic nanoparticles 761:injection and size of 615:inositol hexaphosphate 533:tumor suppressor genes 499:fast track designation 365:tumour suppressor gene 349:p53 activation therapy 307:Clostridium sporogenes 248:Later studies, called 234:maximum tolerated dose 3333:Disruptive innovation 3242:Regenerative medicine 3237:Personalized medicine 3099:Emerging technologies 3016:Carcinogenic bacteria 2756:Malignant progression 827:Tumor Treating Fields 786:Tumor Treating Fields 755:magnetic hyperthermia 739:Magnetic Hyperthermia 729:magnetic hyperthermia 676:Further information: 630:human clinical trials 622:telomerase inhibitors 545:effective treatment. 521:Further information: 501:to ostarine for AR+, 491:clinical benefit rate 435:antifungal medication 3380:Technological change 3323:Collingridge dilemma 2969:Dukes classification 1817:10.3892/ijo_00000702 852:alternative medicine 678:Hyperthermia therapy 658:Photodynamic therapy 653:Photodynamic therapy 487:immunohistochemistry 445:in a similar way to 412:clinical development 404:Boehringer Ingelheim 268:Bacterial treatments 3437:Technology scouting 3412:Accelerating change 3181:Genetic engineering 2788:Sentinel lymph node 2471:2013NYASA1291...86D 2416:2015PLoSO..1030350W 1893:10.1093/jnci/dji010 1757:2008PLoSO...3.2917K 1308:10.2147/OTT.S223119 1109:10.1038/nature05529 1062:10.1038/nature05541 702:heat shock response 686:and coagulation of 648:Radiation therapies 181:regulatory approval 3454:Technology roadmap 3274:Synthetic genomics 3264:Relational biology 3252:Tissue engineering 3176:Generative biology 2836:Respiratory system 2664:clinicaltrials.gov 2479:10.1111/nyas.12112 2195:on 2 November 2007 2159:10.1002/cncr.23155 1571:(15_suppl): 1020. 879:The New York Times 775:Gold nanoparticles 568:Epigenetic options 280:anaerobic bacteria 143:mainstream medical 3487: 3486: 3306: 3305: 3269:Synthetic biology 3247:Stem-cell therapy 3230:engineered uterus 3144:Artificial organs 3065: 3064: 3052:Cancer and nausea 2931: 2930: 2768:Carcinoma in situ 2377:10.1116/1.4915264 1651:10.1172/JCI146777 1613:. 10 January 2022 985:978-0-387-74086-7 952:978-1-904455-38-7 904:(22): 3794–3804. 725:induction heating 706:radiation therapy 634:Geron Corporation 467:estrogen receptor 463:androgen receptor 439:fungal infections 408:anti-cancer agent 285:Clostridium novyi 134: 133: 110: 16:(Redirected from 3507: 3475: 3474: 3422:Horizon scanning 3338:Ephemeralization 3166:Brain transplant 3110: 3092: 3085: 3078: 3069: 2866:Endocrine system 2831:Digestive system 2720: 2693: 2686: 2679: 2670: 2647: 2646: 2620: 2600: 2594: 2593: 2561: 2555: 2546: 2540: 2539: 2529: 2505: 2499: 2498: 2454: 2448: 2447: 2437: 2427: 2395: 2389: 2388: 2360: 2354: 2353: 2343: 2319: 2313: 2312: 2276: 2270: 2269: 2267: 2265: 2254: 2248: 2247: 2211: 2205: 2204: 2202: 2200: 2185: 2179: 2178: 2141: 2135: 2134: 2132: 2130: 2115: 2109: 2108: 2086: 2080: 2079: 2069: 2045: 2039: 2038: 2020: 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2792: 2751: 2711: 2697: 2655: 2650: 2618:10.1.1.521.2180 2602: 2601: 2597: 2576:(13): 2505–14. 2563: 2562: 2558: 2547: 2543: 2507: 2506: 2502: 2456: 2455: 2451: 2410:(7): e0130350. 2397: 2396: 2392: 2362: 2361: 2357: 2321: 2320: 2316: 2287:(12): 1525–38. 2278: 2277: 2273: 2263: 2261: 2260:. ted.com. 2012 2256: 2255: 2251: 2222:(8): 1099–106. 2213: 2212: 2208: 2198: 2196: 2187: 2186: 2182: 2153:(12): 2654–65. 2143: 2142: 2138: 2128: 2126: 2117: 2116: 2112: 2088: 2087: 2083: 2047: 2046: 2042: 1998: 1997: 1993: 1985: 1981: 1976: 1972: 1941: 1940: 1936: 1926: 1924: 1914: 1913: 1909: 1873: 1872: 1868: 1838: 1837: 1833: 1797: 1796: 1792: 1738: 1737: 1733: 1696:Future Oncology 1689: 1688: 1684: 1645:(10): e146777. 1631: 1630: 1626: 1616: 1614: 1605: 1604: 1600: 1558: 1557: 1553: 1509: 1508: 1504: 1450: 1449: 1445: 1401: 1400: 1391: 1347: 1346: 1342: 1288: 1287: 1283: 1261: 1260: 1256: 1226: 1225: 1221: 1186:Nature Medicine 1182: 1181: 1177: 1154:10.1038/nrc2763 1139: 1138: 1134: 1090: 1089: 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2365:Biointerphases 2355: 2314: 2271: 2249: 2206: 2180: 2136: 2110: 2099:(5): 1550088. 2081: 2040: 1991: 1989:on physics.org 1979: 1970: 1934: 1923:on 29 May 2009 1907: 1866: 1831: 1790: 1731: 1682: 1624: 1611:Cancer Network 1598: 1551: 1502: 1443: 1414:(5): 383–391. 1408:The Oncologist 1389: 1340: 1281: 1264:J. 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Oncol 1254: 1219: 1198:10.1038/nm1146 1192:(12): 1321–8. 1175: 1148:(12): 862–73. 1132: 1083: 1040: 1019:(7): 1323–34. 999: 984: 958: 951: 933: 884: 864: 862: 859: 837:Main article: 834: 831: 823: 820: 804: 801: 790:electric field 770: 767: 673: 670: 654: 651: 649: 646: 632:are underway. 605: 602: 569: 566: 518: 515: 459:breast cancers 454: 451: 427: 424: 406:for use as an 393:small molecule 385: 382: 350: 347: 343:bladder cancer 323:Main article: 320: 317: 315: 314:Drug therapies 312: 269: 266: 205:Drug discovery 200: 197: 132: 131: 124: 122: 41: 39: 32: 24: 14: 13: 10: 9: 6: 4: 3: 2: 3512: 3501: 3498: 3497: 3495: 3480: 3479: 3470: 3469: 3466: 3460: 3459:Transhumanism 3457: 3455: 3452: 3450: 3447: 3445: 3442: 3438: 3435: 3433: 3430: 3428: 3425: 3423: 3420: 3418: 3415: 3413: 3410: 3409: 3408: 3405: 3403: 3400: 3398: 3395: 3393: 3390: 3386: 3383: 3382: 3381: 3378: 3376: 3373: 3371: 3368: 3364: 3361: 3359: 3356: 3354: 3351: 3349: 3346: 3345: 3344: 3341: 3339: 3336: 3334: 3331: 3329: 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2333: 2329: 2325: 2318: 2315: 2310: 2306: 2302: 2298: 2294: 2290: 2286: 2282: 2275: 2272: 2259: 2253: 2250: 2245: 2241: 2237: 2233: 2229: 2225: 2221: 2217: 2210: 2207: 2194: 2190: 2184: 2181: 2176: 2172: 2168: 2164: 2160: 2156: 2152: 2148: 2140: 2137: 2125: 2121: 2114: 2111: 2106: 2102: 2098: 2094: 2093: 2085: 2082: 2077: 2073: 2068: 2063: 2060:(4): 151–62. 2059: 2055: 2051: 2044: 2041: 2036: 2032: 2028: 2024: 2019: 2014: 2010: 2006: 2002: 1995: 1992: 1988: 1983: 1980: 1974: 1971: 1966: 1962: 1958: 1954: 1951:(4): 1361–7. 1950: 1946: 1938: 1935: 1922: 1918: 1911: 1908: 1903: 1899: 1894: 1889: 1886:(2): 103–15. 1885: 1881: 1877: 1870: 1867: 1862: 1858: 1854: 1850: 1846: 1842: 1841:Oral Oncology 1835: 1832: 1827: 1823: 1818: 1813: 1809: 1805: 1801: 1794: 1791: 1786: 1782: 1777: 1772: 1767: 1762: 1758: 1754: 1750: 1746: 1742: 1735: 1732: 1727: 1723: 1718: 1713: 1709: 1705: 1702:(1): 137–43. 1701: 1697: 1693: 1686: 1683: 1678: 1674: 1669: 1664: 1660: 1656: 1652: 1648: 1644: 1640: 1636: 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Index

Gene therapy for cancer
reliable medical references
verification
primary sources
add the appropriate references
removed
"Experimental cancer treatment"
news
newspapers
books
scholar
JSTOR
mainstream medical
cancer
surgery
chemotherapy
radiation
immunotherapy
still trying to determine
clinical trials
expanded access
regulatory approval
Health insurance
publicly funded health care
Drug discovery
efficacy
pre-clinical development
Clinical trials
Phase I
maximum tolerated dose

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