Jump to content

Warburg effect (oncology)

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Joek20 (talk | contribs) at 14:24, 11 October 2018 (Fixed again). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

In oncology, the Warburg effect (/ˈvɑːrbʊərɡ/) refers to the observation that cancer cells tend to favor metabolism via aerobic glycolysis rather than the much more efficient oxidative phosphorylation pathway, which is the preference of most other cells of the body. This observation was first made by Nobel laureate Otto Heinrich Warburg.

Basis

Normal cells primarily produce energy through mitochondrial oxidative phosphorylation. However, most cancer cells predominantly produce their energy through a high rate of glycolysis followed by lactic acid fermentation even in the presence of abundant oxygen. This is called aerobic glycolysis, also termed the Warburg effect.[1] Aerobic glycolysis is less efficient than oxidative phosphorylation in terms of adenosine triphosphate production, but leads to the increased generation of additional metabolites that may particularly benefit proliferating cells.[1]

The Warburg effect has been much studied, but its precise nature remains unclear, which hampers the beginning of any work that would explore its therapeutic potential.[2]

Diagnostically the Warburg effect is the basis for the PET scan in which an injected radioactive glucose analog is detected at higher concentrations in malignant cancers than in other tissues.[3]

Otto Warburg postulated this change in metabolism is the fundamental cause of cancer,[4] a claim now known as the Warburg hypothesis. Today, mutations in oncogenes and tumor suppressor genes are thought to be responsible for malignant transformation, and the Warburg effect is considered to be a result of these mutations rather than a cause.[5][6]

Possible explanations

The Warburg effect may simply be a consequence of damage to the mitochondria in cancer, or an adaptation to low-oxygen environments within tumors, or a result of cancer genes shutting down the mitochondria, which are involved in the cell's apoptosis program that kills cancer cells. It may also be an effect associated with cell proliferation. Since glycolysis provides most of the building blocks required for cell proliferation, cancer cells (and normal proliferating cells) have been proposed to need to activate glycolysis, despite the presence of oxygen, to proliferate.[7] Evidence attributes some of the high anaerobic glycolytic rates to an overexpressed form of mitochondrially-bound hexokinase[8] responsible for driving the high glycolytic activity. In kidney cancer, this effect could be due to the presence of mutations in the von Hippel–Lindau tumor suppressor gene upregulating glycolytic enzymes, including the M2 splice isoform of pyruvate kinase.[9] TP53 mutation hits energy metabolism and increases glycolysis in breast cancer.[10]

The Warburg effect is associated with glucose uptake and utilization as this ties into how mitochondrial activity is regulated. The concern lies less in mitochondrial damage and more in the change in activity. On the other hand, tumor cells exhibit increased rates of glycolysis which can be explained with mitochondrial damage.[11]

In March 2008, Lewis C. Cantley and colleagues announced that the tumor M2-PK, a form of the pyruvate kinase enzyme, gives rise to the Warburg effect. Tumor M2-PK is produced in all rapidly dividing cells, and is responsible for enabling cancer cells to consume glucose at an accelerated rate; on forcing the cells to switch to pyruvate kinase's alternative form by inhibiting the production of tumor M2-PK, their growth was curbed. The researchers acknowledged the fact that the exact chemistry of glucose metabolism was likely to vary across different forms of cancer; but PKM2 was identified in all of the cancer cells they had tested. This enzyme form is not usually found in healthy tissue, though it is apparently necessary when cells need to multiply quickly, e.g. in healing wounds or hematopoiesis.[12][13]

Glycolytic inhibitors

Many substances have been developed which inhibit glycolysis, and such inhibitors are currently the subject of intense research as anticancer agents,[14] including SB-204990, 2-deoxy-D-glucose (2DG), 3-bromopyruvate (3-BrPA, bromopyruvic acid, or bromopyruvate), 3-bromo-2-oxopropionate-1-propyl ester (3-BrOP), 5-thioglucose and dichloroacetic acid (DCA). Clinical trial for 2-DG [2008] showed slow accrual and was terminated.[15] There is no evidence yet [2012] to support the use of DCA for cancer treatment.[16]

Alpha-cyano-4-hydroxycinnamic acid (ACCA;CHC), a small-molecule inhibitor of monocarboxylate transporters (MCTs; which prevent lactic acid build up in tumors) has been successfully used as a metabolic target in brain tumor pre-clinical research.[17][18][19][20] Higher affinity MCT inhibitors have been developed and are currently undergoing clinical trials by Astra-Zeneca.[21]

Dichloroacetic acid (DCA), a small-molecule inhibitor of mitochondrial pyruvate dehydrogenase kinase, "downregulates" glycolysis in vitro and in vivo. Researchers at the University of Alberta theorized in 2007 that DCA might have therapeutic benefits against many types of cancer.[22][23]


Pyruvate dehydrogenase catalyses the rate-limiting step in the aerobic oxidation of glucose and pyruvate and links glycolysis to the tricarboxylic acid cycle (TCA). DCA acts a structural analog of pyruvate and activates the pyruvate dehydrogenase complex (PDC) to inhibit pyruvate dehydrogenase kinases, to keep the complex in its un-phosphorylated form. DCA reduces expression of the kinases, preventing the inactivation of the PDC, allowing the conversion of pyruvate to acetyl-CoA rather than lactate through anaerobic respiration, thereby permitting cellular respiration to continue. Through this mechanism of action, DCA works to counteract the increased production of lactate exhibited by tumor cells by enabling the TCA cycle to metabolse it by oxidative phosphorylation. [24] DCA has not been evaluated as a sole cancer treatment yet, as research on the clinical activity of the drug is still in progress, but it has been shown to be effective when used with other cancer treatments. The neurotoxicity and pharmacokinetics of the drug still need to be monitored but if its evaluations are satisfactory it could be very useful as it is an inexpensive small molecule. [25]


Blood glucose levels

High glucose levels have been shown to accelerate cancer cell proliferation in vitro, while glucose deprivation has led to apoptosis. These findings have initiated further study of the effects of carbohydrate restriction on tumor growth. Clinical evidence shows that lower blood glucose levels in late-stage cancer patients have been correlated with better outcomes.[26]

Alternative models

A model called the "reverse Warburg effect" describes cells producing energy by glycolysis, but which are not tumor cells, but stromal fibroblasts.[27] In this scenario, the stroma become corrupted by cancer cells and turn into factories for the synthesis of energy rich nutrients. The cells then take these energy rich nutrients and use them for TCA cycle which is used for oxidative phosphorylation. This results in an energy rich environment that allows for replication of the cancer cells. This still supports Warburg's original observation that tumors show a tendency to create energy through aerobic glycolysis. [28]

Cancer metabolism and epigenetics

Nutrient utilization is dramatically altered when cells receive signals to proliferate. Characteristic metabolic changes enable cells to meet the large biosynthetic demands associated with cell growth and division. Changes in rate-limiting glycolytic enzymes redirect metabolism to support growth and proliferation. Metabolic reprogramming in cancer is largely due to oncogenic activation of signal transduction pathways and transcription factors. Although less well understood, epigenetic mechanisms also contribute to the regulation of metabolic gene expression in cancer. Reciprocally, accumulating evidence suggest that metabolic alterations may affect the epigenome. Understanding the relation between metabolism and epigenetics in cancer cells may open new avenues for anti-cancer strategies.[29]

Drug research

As of 2013, scientists had been investigating the possibility of therapeutic value presented by the Warburg effect. The increase in nutrient uptake by cancer cells has been considered as a possible treatment target by exploitation of a critical proliferation tool in cancer, but it remains unclear whether this can lead to the development of drugs which have therapeutic benefit.[30]

Research by Otto Warburg

Around the 1920s, Otto Warburg and his group of colleagues were able to conclude that by depriving tumor cells of glucose and oxygen, they would be able to deprive tumor cells of energy. By depriving the tumor cells of energy, this is how they would kill the tumor cell. Another biochemist name Herbert Crabtree further extended Warburg's research by discovering that perhaps because of environmental or genetic influence, there is variability in fermentation as well as aerobic glycolysis. Warburg also hypothesized that dysfunctional mitochondria was the source of anaerobic glycolysis, which he also hypothesized was the source of cancer.[2]

References

  1. ^ a b Vander Heiden MG, Cantley LC, Thompson CB (May 2009). "Understanding the Warburg effect: the metabolic requirements of cell proliferation". Science. 324 (5930): 1029–33. Bibcode:2009Sci...324.1029V. doi:10.1126/science.1160809. PMC 2849637. PMID 19460998.
  2. ^ a b Liberti MV, Locasale JW (March 2016). "The Warburg Effect: How Does it Benefit Cancer Cells?". Trends in Biochemical Sciences (Review). 41 (3): 211–218. doi:10.1016/j.tibs.2015.12.001. PMC 4783224. PMID 26778478.
  3. ^ Batra, Surabhi, Kehinde U. A. Adekola, Steven T. Rosen, and Mala Shanmugam. “Cancer Metabolism as a Therapeutic Target.” Oncology (Williston Park, N.Y.) 27, no. 5 (May 2013): 460–67.
  4. ^ Warburg O (February 1956). "On the origin of cancer cells". Science. 123 (3191): 309–14. Bibcode:1956Sci...123..309W. doi:10.1126/science.123.3191.309. PMID 13298683.
  5. ^ Bertram JS (December 2000). "The molecular biology of cancer". Molecular Aspects of Medicine. 21 (6): 167–223. doi:10.1016/S0098-2997(00)00007-8. PMID 11173079.
  6. ^ Grandér D (April 1998). "How do mutated oncogenes and tumor suppressor genes cause cancer?". Medical Oncology. 15 (1): 20–6. doi:10.1007/BF02787340. PMID 9643526.
  7. ^ López-Lázaro M (April 2008). "The warburg effect: why and how do cancer cells activate glycolysis in the presence of oxygen?". Anti-Cancer Agents in Medicinal Chemistry. 8 (3): 305–12. doi:10.2174/187152008783961932. PMID 18393789.
  8. ^ Bustamante E, Pedersen PL (September 1977). "High aerobic glycolysis of rat hepatoma cells in culture: role of mitochondrial hexokinase". Proceedings of the National Academy of Sciences of the United States of America. 74 (9): 3735–9. Bibcode:1977PNAS...74.3735B. doi:10.1073/pnas.74.9.3735. PMC 431708. PMID 198801.
  9. ^ Unwin RD, Craven RA, Harnden P, Hanrahan S, Totty N, Knowles M, Eardley I, Selby PJ, Banks RE (August 2003). "Proteomic changes in renal cancer and co-ordinate demonstration of both the glycolytic and mitochondrial aspects of the Warburg effect". Proteomics. 3 (8): 1620–32. doi:10.1002/pmic.200300464. PMID 12923786.
  10. ^ Harami-Papp H, Pongor LS, Munkácsy G, Horváth G, Nagy ÁM, Ambrus A, Hauser P, Szabó A, Tretter L, Győrffy B (October 2016). "TP53 mutation hits energy metabolism and increases glycolysis in breast cancer". Oncotarget. 7 (41): 67183–67195. doi:10.18632/oncotarget.11594. PMC 5341867. PMID 27582538.
  11. ^ "The Warburg effect and mitochondrial stability in cancer cells". Molecular Aspects of Medicine. 31 (1): 60–74. 2010-02-01. doi:10.1016/j.mam.2009.12.004. ISSN 0098-2997.
  12. ^ Christofk HR, Vander Heiden MG, Harris MH, Ramanathan A, Gerszten RE, Wei R, Fleming MD, Schreiber SL, Cantley LC (March 2008). "The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth". Nature. 452 (7184): 230–3. Bibcode:2008Natur.452..230C. doi:10.1038/nature06734. PMID 18337823.
  13. ^ Pedersen PL (June 2007). "Warburg, me and Hexokinase 2: Multiple discoveries of key molecular events underlying one of cancers' most common phenotypes, the "Warburg Effect", i.e., elevated glycolysis in the presence of oxygen". Journal of Bioenergetics and Biomembranes. 39 (3): 211–22. doi:10.1007/s10863-007-9094-x. PMID 17879147.
  14. ^ Pelicano H, Martin DS, Xu RH, Huang P (August 2006). "Glycolysis inhibition for anticancer treatment". Oncogene. 25 (34): 4633–46. doi:10.1038/sj.onc.1209597. PMID 16892078.
  15. ^ Clinical trial number NCT00633087 for "A Phase I/II Trial of 2-Deoxyglucose (2DG) for the Treatment of Advanced Cancer and Hormone Refractory Prostate Cancer (2-Deoxyglucose)" at ClinicalTrials.gov
  16. ^ "Complementary and Alternative Medicine | American Cancer Society". www.cancer.org. Retrieved 2017-10-18.
  17. ^ Colen, CB (2005). Gene therapy and radiation of malignant glioma by targeting glioma specific lactate transporter (Ph.D.). Wayne State University. {{cite thesis}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)
  18. ^ Colen CB, Seraji-Bozorgzad N, Marples B, Galloway MP, Sloan AE, Mathupala SP (December 2006). "Metabolic remodeling of malignant gliomas for enhanced sensitization during radiotherapy: an in vitro study". Neurosurgery. 59 (6): 1313–23, discussion 1323-4. doi:10.1227/01.NEU.0000249218.65332.BF. PMC 3385862. PMID 17277695.
  19. ^ Colen CB, Shen Y, Ghoddoussi F, Yu P, Francis TB, Koch BJ, Monterey MD, Galloway MP, Sloan AE, Mathupala SP (July 2011). "Metabolic targeting of lactate efflux by malignant glioma inhibits invasiveness and induces necrosis: an in vivo study". Neoplasia. 13 (7): 620–32. doi:10.1593/neo.11134. PMC 3132848. PMID 21750656.
  20. ^ Mathupala SP, Colen CB, Parajuli P, Sloan AE (February 2007). "Lactate and malignant tumors: a therapeutic target at the end stage of glycolysis". Journal of Bioenergetics and Biomembranes. 39 (1): 73–7. doi:10.1007/s10863-006-9062-x. PMC 3385854. PMID 17354062.
  21. ^ Clinical trial number NCT01791595 for "A Phase I Trial of AZD3965 in Patients With Advanced Cancer" at ClinicalTrials.gov
  22. ^ Bonnet S, Archer SL, Allalunis-Turner J, Haromy A, Beaulieu C, Thompson R, Lee CT, Lopaschuk GD, Puttagunta L, Bonnet S, Harry G, Hashimoto K, Porter CJ, Andrade MA, Thebaud B, Michelakis ED (January 2007). "A mitochondria-K+ channel axis is suppressed in cancer and its normalization promotes apoptosis and inhibits cancer growth". Cancer Cell. 11 (1): 37–51. doi:10.1016/j.ccr.2006.10.020. PMID 17222789.
  23. ^ Pan JG, Mak TW (April 2007). "Metabolic targeting as an anticancer strategy: dawn of a new era?". Science's STKE. 2007 (381): pe14. doi:10.1126/stke.3812007pe14. PMID 17426345.
  24. ^ Tran Q, Lee H, Park J, Kim SH, Park J (July 2016). "Targeting Cancer Metabolism - Revisiting the Warburg Effects". Toxicological Research. 32 (3): 177–93. doi:10.5487/TR.2016.32.3.177. PMC 4946416. PMID 27437085.
  25. ^ Michelakis ED, Webster L, Mackey JR (October 2008). "Dichloroacetate (DCA) as a potential metabolic-targeting therapy for cancer". British Journal of Cancer. 99 (7): 989–94. doi:10.1038/sj.bjc.6604554. PMC 2567082. PMID 18766181.
  26. ^ Klement RJ, Kämmerer U (October 2011). "Is there a role for carbohydrate restriction in the treatment and prevention of cancer?". Nutrition & Metabolism. 8: 75. doi:10.1186/1743-7075-8-75. PMC 3267662. PMID 22029671.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  27. ^ Lee M, Yoon JH (August 2015). "Metabolic interplay between glycolysis and mitochondrial oxidation: The reverse Warburg effect and its therapeutic implication". World Journal of Biological Chemistry (Review). 6 (3): 148–61. doi:10.4331/wjbc.v6.i3.148. PMC 4549759. PMID 26322173.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  28. ^ Pavlides, Stephanos (December 1, 2009). "The Reverse Warburg Effect". {{cite web}}: Cite has empty unknown parameter: |dead-url= (help)
  29. ^ Gupta V, Gopinath P, Iqbal MA, Mazurek S, Wellen KE, Bamezai RN (2013). "Interplay between epigenetics & cancer metabolism". Current Pharmaceutical Design. 20 (11): 1706–14. doi:10.2174/13816128113199990536. PMID 23888952.
  30. ^ Vander Heiden MG (September 2013). "Exploiting tumor metabolism: challenges for clinical translation". The Journal of Clinical Investigation. 123 (9): 3648–51. doi:10.1172/JCI72391. PMC 3754281. PMID 23999437.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Warburg_effect_(oncology)&oldid=863553842"