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==Downregulation and upregulation in cancer==
==Downregulation and upregulation in cancer==


DNA damage appears to be the primary underlying cause of cancer.<ref name="pmid18403632">{{cite journal |vauthors=Kastan MB |title=DNA damage responses: mechanisms and roles in human disease: 2007 G.H.A. Clowes Memorial Award Lecture |journal=Mol. Cancer Res. |volume=6 |issue=4 |pages=517–24 |year=2008 |pmid=18403632 |doi=10.1158/1541-7786.MCR-08-0020 |doi-access=free }}</ref><ref name=BernsteinPrasad>{{cite book |last1= Bernstein |first1=C |last2=Prasad |first2=AR |last3=Nfonsam |first3=V |last4=Bernstein |first4=H. |year=2013 |chapter= Chapter 16: DNA Damage, DNA Repair and Cancer |title= New Research Directions in DNA Repair |editor-first=Clark |editor-last=Chen |isbn=978-953-51-1114-6|page=413}}</ref> If accurate DNA repair is deficient, DNA damages tend to accumulate. Unrepaired DNA damage can increase [[mutation]]al errors during [[DNA replication]] due to error-prone [[DNA repair#Translesion synthesis|translesion synthesis]]. DNA damage can also increase [[Epigenetics|epigenetic]] alterations due to errors during DNA repair.<ref name="pmid18704159">{{cite journal | vauthors = O'Hagan HM, Mohammad HP, Baylin SB | title = Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island | journal = PLOS Genet. | volume = 4 | issue = 8 | pages = e1000155 | year = 2008 | pmid = 18704159 | pmc = 2491723 | doi = 10.1371/journal.pgen.1000155 | editor1-last = Lee | editor1-first = Jeannie T }}</ref><ref name="pmid17616978">{{cite journal |vauthors=Cuozzo C, Porcellini A, Angrisano T, Morano A, Lee B, Di Pardo A, Messina S, Iuliano R, Fusco A, Santillo MR, Muller MT, Chiariotti L, Gottesman ME, Avvedimento EV | title = DNA damage, homology-directed repair, and DNA methylation | journal = PLOS Genet. | volume = 3 | issue = 7 | pages = e110 |date=July 2007 | pmid = 17616978 | pmc = 1913100 | doi = 10.1371/journal.pgen.0030110 }}</ref> Such mutations and epigenetic alterations can give rise to [[cancer]] (see [[Neoplasm#Malignant neoplasms|malignant neoplasms]]). Thus, epigenetic downregulation or upregulation of DNA genes that were repaired is likely central to progression to cancer.<ref name=Hagan>{{cite journal |vauthors=O'Hagan HM, Mohammad HP, Baylin SB |title=Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island |journal=PLOS Genetics |volume=4 |issue=8 |pages=e1000155 |year=2008 |pmid=18704159 |pmc=2491723 |doi=10.1371/journal.pgen.1000155}}</ref><ref name=Cuozzo>{{cite journal |vauthors=Cuozzo C, Porcellini A, Angrisano T |title=DNA damage, homology-directed repair, and DNA methylation |journal=PLOS Genetics |volume=3 |issue=7 |pages=e110 | date=July 2007 |pmid=17616978 |pmc=1913100 |doi=10.1371/journal.pgen.0030110|display-authors=etal}}</ref>{{Verify source<!-- Both references supplied talked about the silencing of the genes that were repaired, but the references seem highly technical, someone please check. Clarification also would be appreciated.-->| date = June 2020 }}
DNA damage appears to be the primary underlying cause of cancer.<ref name="pmid18403632">{{cite journal |vauthors=Kastan MB |title=DNA damage responses: mechanisms and roles in human disease: 2007 G.H.A. Clowes Memorial Award Lecture |journal=Mol. Cancer Res. |volume=6 |issue=4 |pages=517–24 |year=2008 |pmid=18403632 |doi=10.1158/1541-7786.MCR-08-0020 |doi-access=free }}</ref><ref name=BernsteinPrasad>{{cite book |last1= Bernstein |first1=C |last2=Prasad |first2=AR |last3=Nfonsam |first3=V |last4=Bernstein |first4=H. |year=2013 |chapter= Chapter 16: DNA Damage, DNA Repair and Cancer |title= New Research Directions in DNA Repair |editor-first=Clark |editor-last=Chen |isbn=978-953-51-1114-6|page=413}}</ref> If accurate DNA repair is deficient, DNA damages tend to accumulate. Unrepaired DNA damage can increase [[mutation]]al errors during [[DNA replication]] due to error-prone [[DNA repair#Translesion synthesis|translesion synthesis]]. DNA damage can also increase [[epigenetic]] alterations due to errors during DNA repair.<ref name="pmid18704159">{{cite journal | vauthors = O'Hagan HM, Mohammad HP, Baylin SB | title = Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island | journal = PLOS Genet. | volume = 4 | issue = 8 | pages = e1000155 | year = 2008 | pmid = 18704159 | pmc = 2491723 | doi = 10.1371/journal.pgen.1000155 | editor1-last = Lee | editor1-first = Jeannie T }}</ref><ref name="pmid17616978">{{cite journal |vauthors=Cuozzo C, Porcellini A, Angrisano T, Morano A, Lee B, Di Pardo A, Messina S, Iuliano R, Fusco A, Santillo MR, Muller MT, Chiariotti L, Gottesman ME, Avvedimento EV | title = DNA damage, homology-directed repair, and DNA methylation | journal = PLOS Genet. | volume = 3 | issue = 7 | pages = e110 |date=July 2007 | pmid = 17616978 | pmc = 1913100 | doi = 10.1371/journal.pgen.0030110 }}</ref> Such mutations and epigenetic alterations can give rise to [[cancer]] (see [[Neoplasm#Malignant neoplasms|malignant neoplasms]]).<ref name=Hagan>{{cite journal |vauthors=O'Hagan HM, Mohammad HP, Baylin SB |title=Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island|quote=Taken together, our data suggest that normal repair of a DNA break can occasionally cause heritable silencing of a CpG island–containing promoter by recruitment of proteins involved in silencing...This finding suggests that DNA damage may directly contribute to the large number of epigenetically silenced genes in tumors. |journal=PLOS Genetics |volume=4 |issue=8 |pages=e1000155 |year=2008 |pmid=18704159 |pmc=2491723 |doi=10.1371/journal.pgen.1000155}}</ref><ref name=Cuozzo>{{cite journal|quote=...data support a mechanistic link between HR and DNA methylation and suggest that DNA methylation in eukaryotes marks homologous recombined segments. |vauthors=Cuozzo C, Porcellini A, Angrisano T |title=DNA damage, homology-directed repair, and DNA methylation |journal=PLOS Genetics |volume=3 |issue=7 |pages=e110 | date=July 2007 |pmid=17616978 |pmc=1913100 |doi=10.1371/journal.pgen.0030110|display-authors=etal}}</ref>{{Verify source<!-- Both references supplied talked about the silencing of the genes that were repaired, but the references seem highly technical, someone please check. Clarification also would be appreciated. [Note from 2nd editor in July 2022: added quotes to cites, but changed statement from "is likely central to progression to cancer" as that is too strong going by sources used.]-->| date = June 2020 }} Investigation of epigenetic down- or upregulation of repaired DNA genes as possibly central to progression of cancer has been regularly undertaken since 2000.<ref>{{cite journal |last1=Baxter |first1=Eva |last2=Windloch |first2=Karolina |last3=Gannon |first3=Frank |last4=Lee |first4=Jason S |title=Epigenetic regulation in cancer progression |journal=Cell & Bioscience |date=December 2014 |volume=4 |issue=1 |pages=45 |doi=10.1186/2045-3701-4-45}}</ref>


As described in [[Regulation of transcription in cancer]], epigenetic downregulation of the DNA repair gene ''[[O-6-methylguanine-DNA methyltransferase|MGMT]]'' occurs in 93% of bladder cancers, 88% of stomach cancers, 74% of thyroid cancers, 40&ndash;90% of colorectal cancers and 50% of brain cancers.{{Citation needed|date=December 2019|reason=removed citation to predatory publisher content}} Similarly, epigenetic downregulation of ''[[LIG4]]'' occurs in 82% of colorectal cancers and epigenetic downregulation of ''[[NEIL1]]'' occurs in 62% of [[head and neck cancer]]s and in 42% of [[non-small-cell lung carcinoma|non-small-cell lung cancer]]s.
As described in [[Regulation of transcription in cancer]], epigenetic downregulation of the DNA repair gene ''[[O-6-methylguanine-DNA methyltransferase|MGMT]]'' occurs in 93% of bladder cancers,<ref>{{cite journal |last1=Bilgrami |first1=Shumaila M |last2=Qureshi |first2=Sohail A |last3=Pervez |first3=Shahid |last4=Abbas |first4=Farhat |title=Promoter hypermethylation of tumor suppressor genes correlates with tumor grade and invasiveness in patients with urothelial bladder cancer |journal=SpringerPlus |date=December 2014 |volume=3 |issue=1 |pages=178 |doi=10.1186/2193-1801-3-178}}</ref> 88% of stomach cancers, 74% of thyroid cancers, 40&ndash;90% of colorectal cancers and 50% of brain cancers.{{Citation needed|date=December 2019|reason=removed citation to predatory publisher content}} Similarly, epigenetic downregulation of ''[[LIG4]]'' occurs in 82% of colorectal cancers and epigenetic downregulation of ''[[NEIL1]]'' occurs in 62% of [[head and neck cancer]]s and in 42% of [[non-small-cell lung carcinoma|non-small-cell lung cancer]]s.


Epigenetic upregulation of the DNA repair genes ''[[PARP1]]'' and ''[[FEN1]]'' occurs in numerous cancers (see [[Regulation of transcription in cancer]]). ''PARP1'' and ''FEN1'' are essential genes in the error-prone and mutagenic DNA repair pathway [[microhomology-mediated end joining]]. If this pathway is upregulated, the excess mutations it causes can lead to cancer. [[PARP1]] is over-expressed in tyrosine kinase-activated leukemias, in neuroblastoma, in testicular and other germ cell tumors, and in Ewing's sarcoma.{{Citation needed|date=December 2019|reason=removed citation to predatory publisher content}} [[FEN1]] is upregulated in the majority of cancers of the breast, prostate, stomach, neuroblastomas, pancreas, and lung.{{Citation needed|date=December 2019|reason=removed citation to predatory publisher content}}
Epigenetic upregulation of the DNA repair genes ''[[PARP1]]'' and ''[[FEN1]]'' occurs in numerous cancers (see [[Regulation of transcription in cancer]]). ''PARP1'' and ''FEN1'' are essential genes in the error-prone and mutagenic DNA repair pathway [[microhomology-mediated end joining]]. If this pathway is upregulated, the excess mutations it causes can lead to cancer. [[PARP1]] is over-expressed in tyrosine kinase-activated leukemias,<ref>{{cite journal |last1=Muvarak |first1=Nidal |last2=Kelley |first2=Shannon |last3=Robert |first3=Carine |last4=Baer |first4=Maria R. |last5=Perrotti |first5=Danilo |last6=Gambacorti-Passerini |first6=Carlo |last7=Civin |first7=Curt |last8=Scheibner |first8=Kara |last9=Rassool |first9=Feyruz V. |title=c-MYC Generates Repair Errors via Increased Transcription of Alternative-NHEJ Factors, LIG3 and PARP1, in Tyrosine Kinase–Activated Leukemias |journal=Molecular Cancer Research |date=1 April 2015 |volume=13 |issue=4 |pages=699–712 |doi=10.1158/1541-7786.MCR-14-0422}}</ref> in neuroblastoma,<ref>{{cite journal |last1=Newman |first1=Erika A. |last2=Lu |first2=Fujia |last3=Bashllari |first3=Daniela |last4=Wang |first4=Li |last5=Opipari |first5=Anthony W. |last6=Castle |first6=Valerie P. |title=Alternative NHEJ Pathway Components Are Therapeutic Targets in High-Risk Neuroblastoma |journal=Molecular Cancer Research |date=1 March 2015 |volume=13 |issue=3 |pages=470–482 |doi=10.1158/1541-7786.MCR-14-0337}}</ref> in testicular and other germ cell tumors,<ref>{{cite journal |last1=Mego |first1=Michal |last2=Cierna |first2=Zuzana |last3=Svetlovska |first3=Daniela |last4=Macak |first4=Dusan |last5=Machalekova |first5=Katarina |last6=Miskovska |first6=Viera |last7=Chovanec |first7=Michal |last8=Usakova |first8=Vanda |last9=Obertova |first9=Jana |last10=Babal |first10=Pavel |last11=Mardiak |first11=Jozef |title=PARP expression in germ cell tumours |journal=Journal of Clinical Pathology |date=July 2013 |volume=66 |issue=7 |pages=607–612 |doi=10.1136/jclinpath-2012-201088}}</ref> and in Ewing's sarcoma.<ref>{{cite journal |last1=Newman |first1=Robert |last2=Soldatenkov |first2=Viatcheslav |last3=Dritschilo |first3=Anatoly |last4=Notario |first4=Vicente |title=Poly(ADP-ribose) polymerase turnover alterations do not contribute to PARP overexpression in Ewing's sarcoma cells |journal=Oncology Reports |date=1 May 2002 |doi=10.3892/or.9.3.529}}</ref> [[FEN1]] is upregulated in the majority of cancers of the breast, prostate, stomach, neuroblastomas, pancreas, and lung.{{Citation needed|date=December 2019|reason=removed citation to predatory publisher content}}


==See also==
==See also==

Revision as of 03:51, 21 July 2022

In the biological context of organisms' production of gene products, downregulation is the process by which a cell decreases the quantity of a cellular component, such as RNA or protein, in response to an external stimulus. The complementary process that involves increases of such components is called upregulation.

An example of downregulation is the cellular decrease in the expression of a specific receptor in response to its increased activation by a molecule, such as a hormone or neurotransmitter, which reduces the cell's sensitivity to the molecule. This is an example of a locally acting (negative feedback) mechanism.

An example of upregulation is the response of liver cells exposed to such xenobiotic molecules as dioxin. In this situation, the cells increase their production of cytochrome P450 enzymes, which in turn increases degradation of these dioxin molecules.

Downregulation or upregulation of an RNA or protein may also arise by an epigenetic alteration. Such an epigenetic alteration can cause expression of the RNA or protein to no longer respond to an external stimulus. This occurs, for instance, during drug addiction or progression to cancer.

Downregulation and upregulation of receptors

All living cells have the ability to receive and process signals that originate outside their membranes, which they do by means of proteins called receptors, often located at the cell's surface imbedded in the plasma membrane. When such signals interact with a receptor, they effectively direct the cell to do something, such as dividing, dying, or allowing substances to be created, or to enter or exit the cell. A cell's ability to respond to a chemical message depends on the presence of receptors tuned to that message. The more receptors a cell has that are tuned to the message, the more the cell will respond to it.

Receptors are created, or expressed, from instructions in the DNA of the cell, and they can be increased, or upregulated, when the signal is weak, or decreased, or downregulated, when it is strong.[1] Their level can also be up or down regulated by modulation of systems that degrade receptors when they are no longer required by the cell.

Downregulation of receptors can also occur when receptors have been chronically exposed to an excessive amount of a ligand, either from endogenous mediators or from exogenous drugs. This results in ligand-induced desensitization or internalization of that receptor. This is typically seen in animal hormone receptors. Upregulation of receptors, on the other hand, can result in super-sensitized cells especially after repeated exposure to an antagonistic drug or prolonged absence of the ligand.

Some receptor agonists may cause downregulation of their respective receptors, while most receptor antagonists temporarily upregulate their respective receptors. The disequilibrium caused by these changes often causes withdrawal when the long-term use of a drug is discontinued.

Upregulation and downregulation can also happen as a response to toxins or hormones. An example of upregulation in pregnancy is hormones that cause cells in the uterus to become more sensitive to oxytocin.

Example: Insulin receptor downregulation

Elevated levels of the hormone insulin in the blood trigger downregulation of the associated receptors.[2] When insulin binds to its receptors on the surface of a cell, the hormone receptor complex undergoes endocytosis and is subsequently attacked by intracellular lysosomal enzymes.[3] The internalization of the insulin molecules provides a pathway for degradation of the hormone as well as for regulation of the number of sites that are available for binding on the cell surface.[4] At high plasma concentrations, the number of surface receptors for insulin is gradually reduced by the accelerated rate of receptor internalization and degradation brought about by increased hormonal binding.[5] The rate of synthesis of new receptors within the endoplasmic reticulum and their insertion in the plasma membrane do not keep pace with their rate of destruction. Over time, this self-induced loss of target cell receptors for insulin reduces the target cell's sensitivity to the elevated hormone concentration.[5]

This process is illustrated by the insulin receptor sites on target cells, e.g. liver cells, in a person with type 2 diabetes.[6] Due to the elevated levels of blood glucose in an overweight individual, the β-cells (islets of Langerhans) in the pancreas must release more insulin than normal to meet the demand and return the blood to homeostatic levels.[7] The near-constant increase in blood insulin levels results from an effort to match the increase in blood glucose, which will cause receptor sites on the liver cells to downregulate and decrease the number of receptors for insulin, increasing the subject's resistance by decreasing sensitivity to this hormone.[citation needed] There is also a hepatic decrease in sensitivity to insulin. This can be seen in the continuing gluconeogenesis in the liver even when blood glucose levels are elevated. This is the more common process of insulin resistance, which leads to adult-onset diabetes.[8]

Another example can be seen in diabetes insipidus, in which the kidneys become insensitive to arginine vasopressin.

Downregulation and upregulation in drug addiction

Family-based, adoption, and twin studies have indicated that there is a strong ( 50%) heritable component to vulnerability to substance abuse addiction.[9]

Especially among genetically vulnerable individuals, repeated exposure to a drug of abuse in adolescence or adulthood causes addiction by inducing stable downregulation or upregulation in expression of specific genes and microRNAs through epigenetic alterations.[10] Such downregulation or upregulation has been shown to occur in the brain's reward regions, such as the nucleus accumbens.[10] (See, for example, Epigenetics of cocaine addiction.)

Downregulation and upregulation in cancer

DNA damage appears to be the primary underlying cause of cancer.[11][12] If accurate DNA repair is deficient, DNA damages tend to accumulate. Unrepaired DNA damage can increase mutational errors during DNA replication due to error-prone translesion synthesis. DNA damage can also increase epigenetic alterations due to errors during DNA repair.[13][14] Such mutations and epigenetic alterations can give rise to cancer (see malignant neoplasms).[15][16][verification needed] Investigation of epigenetic down- or upregulation of repaired DNA genes as possibly central to progression of cancer has been regularly undertaken since 2000.[17]

As described in Regulation of transcription in cancer, epigenetic downregulation of the DNA repair gene MGMT occurs in 93% of bladder cancers,[18] 88% of stomach cancers, 74% of thyroid cancers, 40–90% of colorectal cancers and 50% of brain cancers.[citation needed] Similarly, epigenetic downregulation of LIG4 occurs in 82% of colorectal cancers and epigenetic downregulation of NEIL1 occurs in 62% of head and neck cancers and in 42% of non-small-cell lung cancers.

Epigenetic upregulation of the DNA repair genes PARP1 and FEN1 occurs in numerous cancers (see Regulation of transcription in cancer). PARP1 and FEN1 are essential genes in the error-prone and mutagenic DNA repair pathway microhomology-mediated end joining. If this pathway is upregulated, the excess mutations it causes can lead to cancer. PARP1 is over-expressed in tyrosine kinase-activated leukemias,[19] in neuroblastoma,[20] in testicular and other germ cell tumors,[21] and in Ewing's sarcoma.[22] FEN1 is upregulated in the majority of cancers of the breast, prostate, stomach, neuroblastomas, pancreas, and lung.[citation needed]

See also

References

  1. ^ "Explain To Me: Receptor Upregulation/Downregulation". Retrieved 7 January 2017.
  2. ^ "On the Mechanism of Ligand-induced Down-Regulation of Insulin Receptor Level in the Liver Cel". The Journal of Biological Chemistry. 256.
  3. ^ Zaliauskiene, Lolita; Kang, Sunghyun; Brouillette, Christie G.; Lebowitz, Jacob; Arani, Ramin B.; Collawn, James F. (2016). "Down-Regulation of Cell Surface Receptors Is Modulated by Polar Residues within the Transmembrane Domain". Molecular Biology of the Cell. 11 (8): 2643–2655. doi:10.1091/mbc.11.8.2643. ISSN 1059-1524. PMC 14946. PMID 10930460.
  4. ^ Carpentier, J.-L. (1994). "Insulin receptor internalization: molecular mechanisms and physiopathological implications". Diabetologia. 37 (2): S117–S124. doi:10.1007/BF00400835. ISSN 0012-186X. PMID 7821727.
  5. ^ a b Sherwood, Lauralee; Klandorf, Hillar; Yancey, Paul (2012-01-01). Animal Physiology: From Genes to Organisms. Cengage Learning. ISBN 978-1133709510.
  6. ^ Fröjdö, Sara; Vidal, Hubert; Pirola, Luciano (2009-02-01). "Alterations of insulin signaling in type 2 diabetes: A review of the current evidence from humans". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1792 (2): 83–92. doi:10.1016/j.bbadis.2008.10.019. PMID 19041393.
  7. ^ Wilcox, Gisela (2016-11-20). "Insulin and Insulin Resistance". Clinical Biochemist Reviews. 26 (2): 19–39. ISSN 0159-8090. PMC 1204764. PMID 16278749.
  8. ^ "Protein Controversies in Diabetes". journal.diabetes.org. Retrieved 2016-11-20.
  9. ^ Walker DM, Nestler EJ (2018). "Neuroepigenetics and addiction". Neurogenetics, Part II. Handbook of Clinical Neurology. Vol. 148. pp. 747–765. doi:10.1016/B978-0-444-64076-5.00048-X. ISBN 9780444640765. PMC 5868351. PMID 29478612. {{cite book}}: |journal= ignored (help)
  10. ^ a b Nestler EJ (January 2014). "Epigenetic mechanisms of drug addiction". Neuropharmacology. 76 Pt B: 259–68. doi:10.1016/j.neuropharm.2013.04.004. PMC 3766384. PMID 23643695.
  11. ^ Kastan MB (2008). "DNA damage responses: mechanisms and roles in human disease: 2007 G.H.A. Clowes Memorial Award Lecture". Mol. Cancer Res. 6 (4): 517–24. doi:10.1158/1541-7786.MCR-08-0020. PMID 18403632.
  12. ^ Bernstein, C; Prasad, AR; Nfonsam, V; Bernstein, H. (2013). "Chapter 16: DNA Damage, DNA Repair and Cancer". In Chen, Clark (ed.). New Research Directions in DNA Repair. p. 413. ISBN 978-953-51-1114-6.
  13. ^ O'Hagan HM, Mohammad HP, Baylin SB (2008). Lee JT (ed.). "Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island". PLOS Genet. 4 (8): e1000155. doi:10.1371/journal.pgen.1000155. PMC 2491723. PMID 18704159.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  14. ^ Cuozzo C, Porcellini A, Angrisano T, Morano A, Lee B, Di Pardo A, Messina S, Iuliano R, Fusco A, Santillo MR, Muller MT, Chiariotti L, Gottesman ME, Avvedimento EV (July 2007). "DNA damage, homology-directed repair, and DNA methylation". PLOS Genet. 3 (7): e110. doi:10.1371/journal.pgen.0030110. PMC 1913100. PMID 17616978.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  15. ^ O'Hagan HM, Mohammad HP, Baylin SB (2008). "Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island". PLOS Genetics. 4 (8): e1000155. doi:10.1371/journal.pgen.1000155. PMC 2491723. PMID 18704159. Taken together, our data suggest that normal repair of a DNA break can occasionally cause heritable silencing of a CpG island–containing promoter by recruitment of proteins involved in silencing...This finding suggests that DNA damage may directly contribute to the large number of epigenetically silenced genes in tumors.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  16. ^ Cuozzo C, Porcellini A, Angrisano T, et al. (July 2007). "DNA damage, homology-directed repair, and DNA methylation". PLOS Genetics. 3 (7): e110. doi:10.1371/journal.pgen.0030110. PMC 1913100. PMID 17616978. ...data support a mechanistic link between HR and DNA methylation and suggest that DNA methylation in eukaryotes marks homologous recombined segments.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  17. ^ Baxter, Eva; Windloch, Karolina; Gannon, Frank; Lee, Jason S (December 2014). "Epigenetic regulation in cancer progression". Cell & Bioscience. 4 (1): 45. doi:10.1186/2045-3701-4-45.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  18. ^ Bilgrami, Shumaila M; Qureshi, Sohail A; Pervez, Shahid; Abbas, Farhat (December 2014). "Promoter hypermethylation of tumor suppressor genes correlates with tumor grade and invasiveness in patients with urothelial bladder cancer". SpringerPlus. 3 (1): 178. doi:10.1186/2193-1801-3-178.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  19. ^ Muvarak, Nidal; Kelley, Shannon; Robert, Carine; Baer, Maria R.; Perrotti, Danilo; Gambacorti-Passerini, Carlo; Civin, Curt; Scheibner, Kara; Rassool, Feyruz V. (1 April 2015). "c-MYC Generates Repair Errors via Increased Transcription of Alternative-NHEJ Factors, LIG3 and PARP1, in Tyrosine Kinase–Activated Leukemias". Molecular Cancer Research. 13 (4): 699–712. doi:10.1158/1541-7786.MCR-14-0422.
  20. ^ Newman, Erika A.; Lu, Fujia; Bashllari, Daniela; Wang, Li; Opipari, Anthony W.; Castle, Valerie P. (1 March 2015). "Alternative NHEJ Pathway Components Are Therapeutic Targets in High-Risk Neuroblastoma". Molecular Cancer Research. 13 (3): 470–482. doi:10.1158/1541-7786.MCR-14-0337.
  21. ^ Mego, Michal; Cierna, Zuzana; Svetlovska, Daniela; Macak, Dusan; Machalekova, Katarina; Miskovska, Viera; Chovanec, Michal; Usakova, Vanda; Obertova, Jana; Babal, Pavel; Mardiak, Jozef (July 2013). "PARP expression in germ cell tumours". Journal of Clinical Pathology. 66 (7): 607–612. doi:10.1136/jclinpath-2012-201088.
  22. ^ Newman, Robert; Soldatenkov, Viatcheslav; Dritschilo, Anatoly; Notario, Vicente (1 May 2002). "Poly(ADP-ribose) polymerase turnover alterations do not contribute to PARP overexpression in Ewing's sarcoma cells". Oncology Reports. doi:10.3892/or.9.3.529.

Sources

  • Sherwood, L. (2004). Human Physiology From Cells to Systems, 5th Ed (p. 680). Belmont, CA: Brooks/Cole-Thomson Learning
  • Wilmore, J., Costill, D. (2004). Physiology of Sport and Exercise, 3rd Ed (p. 164). Champaign, IL: Human Kinetics

External links

Retrieved from "https://en.wikipedia.org/w/index.php?title=Downregulation_and_upregulation&oldid=1099503390"