Biology:Tumor-homing bacteria
Tumor-homing bacteria are facultative or obligate anaerobic bacteria (capable of producing ATP when oxygen is absent or is destroyed in normal oxygen levels) that are able to target cancerous cells in the body, suppress tumor growth and survive in the body for a long time even after the infection. When this type of bacteria is administered into the body, it migrates to the cancerous tissues and starts to grow, and then deploys distinct mechanisms to destroy solid tumors. Each bacteria species uses a different process to eliminate the tumor. Some common tumor homing bacteria include Salmonella, Clostridium, Bifidobacterium, Listeria, and Streptococcus.[1] The earliest research of this type of bacteria was highlighted in 1813 when scientists began observing that patients that had gas gangrene, an infection caused by the bacteria Clostridium, were able to have tumor regressions.[2]
Tumor-inhibition mechanisms
Different strains of tumor homing bacteria in distinct environments use unique or similar processes to inhibit or destroy tumor growth.
Unique mechanisms
- Salmonella bacteria kill tumor cells by uncontrolled bacterial multiplication that can lead to the bursting of cancerous cells. Moreover, the macrophages and dendritic cells (type of white blood cells) in these Salmonella-colonized tumors secrete IL-1β, a protein responsible for anti-tumor activity.[3]
- S. Typhimurium flagellin increases both innate and adaptive immunity (nonspecific and specific defense mechanisms) of the bacteria by stimulating NK cells (Natural Killer cells) to produce interferon-γ (IFN-γ), an important cytokine (regulatory protein) for this immunity.[1]
- Listeria inhibits tumors through NADPH oxidase mediated production (nicotinamide adenine dinucleotide phosphate oxidase) of ROS (reactive oxygen species) which is a cell signaling process that activates CD8+ T cells (cells that kill cancerous tissue) which target primary tumors.[4]
Similar mechanisms
- Clostridium, S. Typhimurium, Listeria produce exotoxins (e.g. phospholipases, hemolysins, lipases) that damage the membrane structure and the cellular functions of the tumor using apoptosis or autophagy which is programmed cell death.[2]
- Salmonella, Clostridium, and Listeria infections promote tumor elimination by increasing cytokines and chemokines (cell signaling regulatory proteins) that regulate infected sites using granulocytes and cytotoxic lymphocytes (WBC s that kill cancerous cells).[1]
Confirmed medical treatments
Bacterial cancer therapy is an emerging field for cancer treatment. Although many clinical trials are taking place, as of right now only a few confirmed treatments are being administered to patients.
Treatment with live strains of bacteria
- The usage of the live attenuated strain of Mycobacterium Bovis, also known as Bacillus Calmette-Guérin (BCG), is a confirmed treatment for bladder cancer. BCG therapy is done by intravesical instillation (drug administration into the urinary bladder via a catheter) and has been used since 1970 on cancer patients.[5]
- Due to the necrotic and hypoxic regions of tumor cells (area of treatment resistance), drug delivery of chemotherapy can be impaired. Therefore Salmonella can be combined with chemotherapy to provide treatment and transport as Salmonella is not affected by these regions. Moreover, the Salmonella mutant strain VNP20009 increased in number from this combination which causes further inhibition of cancerous cells by stimulating anti-tumor proteins.[6]
Treatment with genetically engineered bacteria
Tumor homing bacteria can be genetically engineered to enhance their anti-tumor activities and be used to transport therapeutic materials based on medical needs.[7] They are usually transformed into a plasmid that contains the specific gene expression of these therapeutic proteins of the bacteria. After the plasmid reaches the target site, the protein’s genetic sequence is expressed and the bacteria can have its full biological effect. Currently, there is no approved treatment with genetically engineered bacteria. However, research is being conducted on Listeria and Clostridium as vectors to transport RNAi (suppresses genes) for colon cancer.[8]
Safety
Some active tumor-homing bacteria can be harmful to the human body, since they produce toxins that disturb the cell cycle which results in altered cell growth and chronic infections. However, many ways to enhance the safety of tumor homing bacteria in the body has been found. For example, when the virulent genes of the bacteria are removed by gene targeting, a process where genes are deleted or modified, it can be reduced in pathogenicity[citation needed] (property of causing disease).
Adverse effects
- DNA mutations of the tumor homing bacteria in the body can lead to problems like extreme infection and failure of therapy as the genes that are expressed will be different and cause the bacteria to become non-functional.
- Incomplete tumor lysis or colonization by the bacteria can lead to delayed treatment and will necessitate the use of other cancer treatments such as chemotherapy or a combination of more. Delayed or combined treatment causes many effects on the body such as vomiting, nausea, loss of appetite, fatigue, and hair loss.[9]
Prevention of adverse effects
- Deleting the msbB gene from Salmonella by genetic engineering leads to the loss of lipid A (a lipid responsible for the toxicity levels of gram-negative bacteria) and therefore reduces the toxicity of Salmonella by 10,000-fold.[10]
- Generating auxotrophic mutants (a strain of microorganism that will proliferate only when the medium is supplemented with some specific substance) that cannot replicate efficiently in an environment where a particular nutrient required by the mutant strain is scarce. Salmonella A1-R represents such a strain, which is auxotrophic for the amino acids leucine and arginine that are enriched in the tumor but not in normal tissues. Therefore in the tumor, Salmonella A1-R will grow but not in the normal tissues thereby preventing infections and increasing safety.[2]
Research
The most researched bacteria for cancer therapy are Salmonella, Listeria, and Clostridium. A genetically engineered strain of Salmonella (TAPET-CD) has completed phase 1 clinical trials for patients with stage 4 metastatic cancer.[11] Listeria-based cancer vaccines are currently being produced and are undergoing many clinical trials.[12] Phase I trials of the Clostridium strain called Clostridium novyi (C. novyi-NT) for patients with treatment-refractory tumors or tumors that are unresponsive to treatment is currently underway.[13]
See also
References
- ↑ 1.0 1.1 1.2 Duong, Mai Thi-Quynh; Qin, Yeshan; You, Sung-Hwan; Min, Jung-Joon (December 2019). "Bacteria-cancer interactions: bacteria-based cancer therapy" (in en). Experimental & Molecular Medicine 51 (12): 1–15. doi:10.1038/s12276-019-0297-0. ISSN 2092-6413. PMID 31827064.
- ↑ 2.0 2.1 2.2 Zhou, Shibin; Gravekamp, Claudia; Bermudes, David; Liu, Ke (December 2018). "Tumor-targeting bacteria engineered to fight cancer". Nature Reviews. Cancer 18 (12): 727–743. doi:10.1038/s41568-018-0070-z. ISSN 1474-175X. PMID 30405213.
- ↑ Kim, Jung-Eun; Phan, Thuy Xuan; Nguyen, Vu Hong; Dinh-Vu, Hong-Van; Zheng, Jin Hai; Yun, Misun; Park, Sung-Gyoo; Hong, Yeongjin et al. (2015). "Salmonella typhimurium Suppresses Tumor Growth via the Pro-Inflammatory Cytokine Interleukin-1β". Theranostics 5 (12): 1328–1342. doi:10.7150/thno.11432. ISSN 1838-7640. PMID 26516371.
- ↑ Kim, Sun Hee; Castro, Francisco; Paterson, Yvonne; Gravekamp, Claudia (2009-07-15). "High Efficacy of a Listeria-Based Vaccine against Metastatic Breast Cancer Reveals a Dual Mode of Action" (in en). Cancer Research 69 (14): 5860–5866. doi:10.1158/0008-5472.CAN-08-4855. ISSN 0008-5472. PMID 19584282.
- ↑ Torres, Wheeler; Lameda, Víctor; Olivar, Luis Carlos; Navarro, Carla; Fuenmayor, Jorge; Pérez, Adrián; Mindiola, Andres; Rojas, Milagros et al. (2018-01-24). "Bacteria in cancer therapy: beyond immunostimulation" (in en-us). Journal of Cancer Metastasis and Treatment 4: 4. doi:10.20517/2394-4722.2017.49. ISSN 2394-4722. https://jcmtjournal.com/article/view/2365.
- ↑ Mi, Ze; Feng, Zhi-Chao; Li, Cheng; Yang, Xiao; Ma, Meng-Tian; Rong, Peng-Fei (2019-08-20). "Salmonella-Mediated Cancer Therapy: An Innovative Therapeutic Strategy". Journal of Cancer 10 (20): 4765–4776. doi:10.7150/jca.32650. ISSN 1837-9664. PMID 31598148.
- ↑ Sieow, Brendan Fu-Long; Wun, Kwok Soon; Yong, Wei Peng; Hwang, In Young; Chang, Matthew Wook (December 2020). "Tweak to Treat: Reprograming Bacteria for Cancer Treatment". Trends in Cancer 7 (5): 447–464. doi:10.1016/j.trecan.2020.11.004. ISSN 2405-8033. PMID 33303401.
- ↑ Chien, Tiffany; Doshi, Anjali; Danino, Tal (October 2017). "Advances in bacterial cancer therapies using synthetic biology". Current Opinion in Systems Biology 5: 1–8. doi:10.1016/j.coisb.2017.05.009. ISSN 2452-3100. PMID 29881788.
- ↑ Patyar, S; Joshi, R; Byrav, DS Prasad; Prakash, A; Medhi, B; Das, BK (2010-03-23). "Bacteria in cancer therapy: a novel experimental strategy". Journal of Biomedical Science 17 (1): 21. doi:10.1186/1423-0127-17-21. ISSN 1021-7770. PMID 20331869.
- ↑ Toso, John F.; Gill, Vee J.; Hwu, Patrick; Marincola, Francesco M.; Restifo, Nicholas P.; Schwartzentruber, Douglas J.; Sherry, Richard M.; Topalian, Suzanne L. et al. (2002-01-01). "Phase I Study of the Intravenous Administration of Attenuated Salmonella typhimurium to Patients With Metastatic Melanoma". Journal of Clinical Oncology 20 (1): 142–152. doi:10.1200/JCO.2002.20.1.142. ISSN 0732-183X. PMID 11773163.
- ↑ Cunningham, C.; Nemunaitis, J. (2001-08-10). "A phase I trial of genetically modified Salmonella typhimurium expressing cytosine deaminase (TAPET-CD, VNP20029) administered by intratumoral injection in combination with 5-fluorocytosine for patients with advanced or metastatic cancer. Protocol no: CL-017. Version: April 9, 2001". Human Gene Therapy 12 (12): 1594–1596. ISSN 1043-0342. PMID 11529249. https://pubmed.ncbi.nlm.nih.gov/11529249/.
- ↑ Flickinger, John C.; Rodeck, Ulrich; Snook, Adam E. (2018-07-25). "Listeria monocytogenes as a Vector for Cancer Immunotherapy: Current Understanding and Progress". Vaccines 6 (3): 48. doi:10.3390/vaccines6030048. ISSN 2076-393X. PMID 30044426.
- ↑ Staedtke, Verena; Roberts, Nicholas J.; Bai, Ren-Yuan; Zhou, Shibin (2016-02-06). "Clostridium novyi-NT in cancer therapy". Genes & Diseases 3 (2): 144–152. doi:10.1016/j.gendis.2016.01.003. ISSN 2352-4820. PMID 30258882.
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