{"id":198,"date":"2014-10-31T15:07:27","date_gmt":"2014-10-31T15:07:27","guid":{"rendered":"http:\/\/courses.candelalearning.com\/novabiology\/?post_type=chapter&#038;p=198"},"modified":"2019-05-13T18:12:34","modified_gmt":"2019-05-13T18:12:34","slug":"cancer-and-the-cell-cycle","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/chapter\/cancer-and-the-cell-cycle\/","title":{"raw":"Cancer and the Cell Cycle","rendered":"Cancer and the Cell Cycle"},"content":{"raw":"<div class=\"textbox learning-objectives\">\r\n<h3>Learning Objectives:<\/h3>\r\nBy the end of this section, you will be able to:\r\n<ul>\r\n \t<li>Describe how cancer is caused by uncontrolled cell growth<\/li>\r\n \t<li>Understand how proto-oncogenes are normal cell genes that, when mutated, become oncogenes<\/li>\r\n \t<li>Describe how tumor suppressors function<\/li>\r\n \t<li>Explain how mutant tumor suppressors cause cancer<\/li>\r\n<\/ul>\r\n<\/div>\r\nCancer comprises many different diseases caused by a common mechanism: uncontrolled cell growth. Despite the redundancy and overlapping levels of cell cycle control, errors do occur.\u00a0 During the S phase, the most critical checkpoint occurs in determining proper DNA replication.\u00a0 Even when all controls are fully functional, a small percentage of replication errors (mutations) will be passed on to the daughter cells. If changes are not corrected, a gene mutation results. All cancers start from a gene mutation giving rise to a faulty protein.\u00a0 The change in the cell that results from the malformed protein may be minor or detrimental. \u00a0 But even minor mistakes may allow further mistakes to readily occur.\u00a0 Small, uncorrected errors are passed from the parent cell to the daughter cells and amplified.\u00a0 Eventually, the pace of the cell cycle increases, as the control and repair mechanisms decreases. Uncontrolled growth of the mutated cells outpaces the growth of normal cells in the area and a tumor (\u201c-oma\u201d) can occur.\r\n<h2>Proto-oncogenes<\/h2>\r\nThe genes coding for the positive cell cycle regulators are called proto-oncogenes. Proto-oncogenes are normal genes when mutated, become oncogenes.\u00a0 Oncogenes cause a cell to become cancerous.\u00a0 What might happen should an oncogene develop?\u00a0 The alteration of the DNA sequence will result in a less functional protein. This would be detrimental to the cell and likely prevent the cell from completing the cell cycle.\u00a0 The organism, as a whole, is not harmed because the mutation will not be carried forward. If a cell cannot reproduce, the mutation is not passed and the damage is minimal.\u00a0 But sometimes, a gene mutation causes a change that increases the activity of a positive regulator. A mutation could push the cell cycle past a checkpoint before all required conditions are met. If the resulting daughter cells undergo further cell divisions, the mutation would be propagated and harm could come to the organism.\r\n\r\nIn addition to the cell cycle regulatory proteins, any protein that influences the cycle can be altered in such a way as to override cell cycle checkpoints. An <span style=\"text-decoration: underline\">oncogene<\/span> is any altered gene that leads to an increase in the rate of cell cycle progression.\r\n<h2>Tumor Suppressor Genes<\/h2>\r\nTumor suppressor genes are segments of DNA that code for negative regulator proteins.\u00a0 Negative regulator proteins, when activated, can prevent the cell from undergoing uncontrolled division.\u00a0 The best understood tumor suppressor gene proteins, Rb, p53, and p21, puts up a roadblock to cell cycle progression until certain events are completed. A cell that carries a mutated form of a negative protein regulator might not be able to halt the cell cycle if there is a problem.\r\n\r\nMutated p53 genes have been identified in more than one-half of all human tumor cells.\u00a0 A cell with a faulty p53 may fail to detect errors present in the genomic DNA (Figure\u00a01).\u00a0 If a partially functional p53 does identify the mutations, the enzymes needed for DNA repair may not be produced. \u00a0 Damaged DNA will remain uncorrected. A functional p53 will deem the cell unsalvageable and trigger programmed cell death (apoptosis).\u00a0 Damaged versions of p53 in cancer cells cannot trigger apoptosis.\r\n<div class=\"textbox key-takeaways\">\r\n<h3>Art Connection<\/h3>\r\n[caption id=\"attachment_1428\" align=\"aligncenter\" width=\"725\"]<img class=\"size-full wp-image-1428\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/198\/2016\/11\/28181646\/Figure_10_04_01.png\" alt=\"Part a: This illustration shows cell cycle regulation by normal p53, which arrests the cell cycle in response to DNA damage, cell cycle abnormalities, or hypoxia. Once the damage is repaired, the cell cycle restarts. If the damage cannot be repaired, apoptosis (programmed cell death) occurs. Part b: Mutated p53 does not arrest the cell cycle in response to cellular damage. As a result, the cell cycle continues, and the cell may become cancerous.\" width=\"725\" height=\"598\" \/> Figure\u00a01. The role of normal p53 is to monitor DNA and the supply of oxygen (hypoxia is a condition of reduced oxygen supply). If damage is detected, p53 triggers repair mechanisms. If repairs are unsuccessful, p53 signals apoptosis. A cell with an abnormal p53 protein cannot repair damaged DNA and thus cannot signal apoptosis. Cells with abnormal p53 can become cancerous. (credit: modification of work by Thierry Soussi)[\/caption]\r\n\r\n<\/div>\r\nOther issues occur for the cell cycle due to mutated\u00a0 p53 function.\u00a0 Without a fully functional p53, the G<sub>1<\/sub> checkpoint is severely compromised and the cell proceeds directly from G<sub>1<\/sub> to S regardless of internal and external conditions. At the completion of this shortened cell cycle, two daughter cells are produced with the mutated p53 gene. It is likely that the daughter cells will have acquired other mutations.\u00a0 Cells such as these quickly accumulate both oncogenes and non-functional tumor suppressor genes.\u00a0 The result is tumor growth.\r\n<div class=\"textbox shaded\">\r\n<h3>Link to Learning<\/h3>\r\nWatch this video\u00a0of how cancer results from errors in the cell cycle:\r\n\r\nhttps:\/\/youtu.be\/RZhL7LDPk8w\r\n\r\n<\/div>\r\n<h2>Section Summary<\/h2>\r\nCancer is the result of unchecked cell division by a breakdown cell cycle regulation.\u00a0 The loss of control begins with a change in the DNA\u00a0 coding for one of the regulatory molecules. Faulty instructions lead to a faulty protein.\u00a0 Any disruption of the monitoring system can allow other mistakes to be passed on. Each successive cell division will give rise to daughter cells with even more accumulated damage. Eventually, all checkpoints become nonfunctional, and rapidly reproducing cells crowd out normal cells.\u00a0 Cancerous tumors result.\r\n\r\nhttps:\/\/www.openassessments.org\/assessments\/476\r\n<div class=\"textbox exercises\">\r\n<h3>Additional Self Check Questions<\/h3>\r\n<ol>\r\n \t<li>Explain the difference between a proto-oncogene and a tumor suppressor gene.<\/li>\r\n \t<li>List the regulatory mechanisms that might be lost in a cell producing faulty p53.<\/li>\r\n \t<li>p53 can trigger apoptosis if certain cell cycle events fail. How does this regulatory outcome benefit a multicellular organism?<\/li>\r\n<\/ol>\r\n<\/div>\r\n<div class=\"textbox exercises\">\r\n<h3>Answers<\/h3>\r\n<ol>\r\n \t<li>A proto-oncogene is a segment of DNA that codes for one of the positive cell cycle regulators. If that gene becomes mutated, it is considered an oncogene. A tumor suppressor gene is a segment of DNA that codes for one of the negative cell cycle regulators. If that gene becomes mutated then the protein product becomes less active and the cell cycle will run unchecked. A single oncogene can initiate abnormal cell divisions.\u00a0 Tumor suppressors lose their effectiveness only when both copies of the gene are damaged.<\/li>\r\n \t<li>Regulatory mechanisms that might be lost include monitoring of the quality of the genomic DNA, recruiting of repair enzymes, and the triggering of apoptosis.<\/li>\r\n \t<li>If a cell has damaged DNA, the likelihood of producing faulty proteins increases. The daughter cells would produce faulty proteins that might eventually become cancerous. If p53 recognizes this damage, it triggers the cell to self-destruct, the damaged DNA is degraded and recycled. No further harm comes to the organism.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<div class=\"textbox key-takeaways\">\r\n<h3>Glossary<\/h3>\r\n<strong>oncogene: <\/strong>mutated version of a normal gene involved in the positive regulation of the cell cycle\r\n\r\n<strong>proto-oncogene: <\/strong>normal gene that when mutated becomes an oncogene\r\n\r\n<strong>tumor suppressor gene: <\/strong>segment of DNA that codes for regulator proteins that prevent the cell from undergoing uncontrolled division\r\n\r\n<\/div>","rendered":"<div class=\"textbox learning-objectives\">\n<h3>Learning Objectives:<\/h3>\n<p>By the end of this section, you will be able to:<\/p>\n<ul>\n<li>Describe how cancer is caused by uncontrolled cell growth<\/li>\n<li>Understand how proto-oncogenes are normal cell genes that, when mutated, become oncogenes<\/li>\n<li>Describe how tumor suppressors function<\/li>\n<li>Explain how mutant tumor suppressors cause cancer<\/li>\n<\/ul>\n<\/div>\n<p>Cancer comprises many different diseases caused by a common mechanism: uncontrolled cell growth. Despite the redundancy and overlapping levels of cell cycle control, errors do occur.\u00a0 During the S phase, the most critical checkpoint occurs in determining proper DNA replication.\u00a0 Even when all controls are fully functional, a small percentage of replication errors (mutations) will be passed on to the daughter cells. If changes are not corrected, a gene mutation results. All cancers start from a gene mutation giving rise to a faulty protein.\u00a0 The change in the cell that results from the malformed protein may be minor or detrimental. \u00a0 But even minor mistakes may allow further mistakes to readily occur.\u00a0 Small, uncorrected errors are passed from the parent cell to the daughter cells and amplified.\u00a0 Eventually, the pace of the cell cycle increases, as the control and repair mechanisms decreases. Uncontrolled growth of the mutated cells outpaces the growth of normal cells in the area and a tumor (\u201c-oma\u201d) can occur.<\/p>\n<h2>Proto-oncogenes<\/h2>\n<p>The genes coding for the positive cell cycle regulators are called proto-oncogenes. Proto-oncogenes are normal genes when mutated, become oncogenes.\u00a0 Oncogenes cause a cell to become cancerous.\u00a0 What might happen should an oncogene develop?\u00a0 The alteration of the DNA sequence will result in a less functional protein. This would be detrimental to the cell and likely prevent the cell from completing the cell cycle.\u00a0 The organism, as a whole, is not harmed because the mutation will not be carried forward. If a cell cannot reproduce, the mutation is not passed and the damage is minimal.\u00a0 But sometimes, a gene mutation causes a change that increases the activity of a positive regulator. A mutation could push the cell cycle past a checkpoint before all required conditions are met. If the resulting daughter cells undergo further cell divisions, the mutation would be propagated and harm could come to the organism.<\/p>\n<p>In addition to the cell cycle regulatory proteins, any protein that influences the cycle can be altered in such a way as to override cell cycle checkpoints. An <span style=\"text-decoration: underline\">oncogene<\/span> is any altered gene that leads to an increase in the rate of cell cycle progression.<\/p>\n<h2>Tumor Suppressor Genes<\/h2>\n<p>Tumor suppressor genes are segments of DNA that code for negative regulator proteins.\u00a0 Negative regulator proteins, when activated, can prevent the cell from undergoing uncontrolled division.\u00a0 The best understood tumor suppressor gene proteins, Rb, p53, and p21, puts up a roadblock to cell cycle progression until certain events are completed. A cell that carries a mutated form of a negative protein regulator might not be able to halt the cell cycle if there is a problem.<\/p>\n<p>Mutated p53 genes have been identified in more than one-half of all human tumor cells.\u00a0 A cell with a faulty p53 may fail to detect errors present in the genomic DNA (Figure\u00a01).\u00a0 If a partially functional p53 does identify the mutations, the enzymes needed for DNA repair may not be produced. \u00a0 Damaged DNA will remain uncorrected. A functional p53 will deem the cell unsalvageable and trigger programmed cell death (apoptosis).\u00a0 Damaged versions of p53 in cancer cells cannot trigger apoptosis.<\/p>\n<div class=\"textbox key-takeaways\">\n<h3>Art Connection<\/h3>\n<div id=\"attachment_1428\" style=\"width: 735px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-1428\" class=\"size-full wp-image-1428\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/198\/2016\/11\/28181646\/Figure_10_04_01.png\" alt=\"Part a: This illustration shows cell cycle regulation by normal p53, which arrests the cell cycle in response to DNA damage, cell cycle abnormalities, or hypoxia. Once the damage is repaired, the cell cycle restarts. If the damage cannot be repaired, apoptosis (programmed cell death) occurs. Part b: Mutated p53 does not arrest the cell cycle in response to cellular damage. As a result, the cell cycle continues, and the cell may become cancerous.\" width=\"725\" height=\"598\" \/><\/p>\n<p id=\"caption-attachment-1428\" class=\"wp-caption-text\">Figure\u00a01. The role of normal p53 is to monitor DNA and the supply of oxygen (hypoxia is a condition of reduced oxygen supply). If damage is detected, p53 triggers repair mechanisms. If repairs are unsuccessful, p53 signals apoptosis. A cell with an abnormal p53 protein cannot repair damaged DNA and thus cannot signal apoptosis. Cells with abnormal p53 can become cancerous. (credit: modification of work by Thierry Soussi)<\/p>\n<\/div>\n<\/div>\n<p>Other issues occur for the cell cycle due to mutated\u00a0 p53 function.\u00a0 Without a fully functional p53, the G<sub>1<\/sub> checkpoint is severely compromised and the cell proceeds directly from G<sub>1<\/sub> to S regardless of internal and external conditions. At the completion of this shortened cell cycle, two daughter cells are produced with the mutated p53 gene. It is likely that the daughter cells will have acquired other mutations.\u00a0 Cells such as these quickly accumulate both oncogenes and non-functional tumor suppressor genes.\u00a0 The result is tumor growth.<\/p>\n<div class=\"textbox shaded\">\n<h3>Link to Learning<\/h3>\n<p>Watch this video\u00a0of how cancer results from errors in the cell cycle:<\/p>\n<p><iframe loading=\"lazy\" id=\"oembed-1\" title=\"Cancer | Cells | MCAT | Khan Academy\" width=\"500\" height=\"281\" src=\"https:\/\/www.youtube.com\/embed\/RZhL7LDPk8w?feature=oembed&#38;rel=0\" frameborder=\"0\" allowfullscreen=\"allowfullscreen\"><\/iframe><\/p>\n<\/div>\n<h2>Section Summary<\/h2>\n<p>Cancer is the result of unchecked cell division by a breakdown cell cycle regulation.\u00a0 The loss of control begins with a change in the DNA\u00a0 coding for one of the regulatory molecules. Faulty instructions lead to a faulty protein.\u00a0 Any disruption of the monitoring system can allow other mistakes to be passed on. Each successive cell division will give rise to daughter cells with even more accumulated damage. Eventually, all checkpoints become nonfunctional, and rapidly reproducing cells crowd out normal cells.\u00a0 Cancerous tumors result.<\/p>\n<p><iframe src=\"https:\/\/lumenoea.herokuapp.com\/assessments\/load?src_url=https:\/\/lumenoea.herokuapp.com\/api\/assessments\/476.xml&#38;results_end_point=https:\/\/lumenoea.herokuapp.com\/api&#38;assessment_id=476&#38;confidence_levels=true&#38;enable_start=true&#38;eid=https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/chapter\/cancer-and-the-cell-cycle\/\" frameborder=\"0\" style=\"border:none;width:100%;height:100%;min-height:400px;\"><\/iframe><\/p>\n<div class=\"textbox exercises\">\n<h3>Additional Self Check Questions<\/h3>\n<ol>\n<li>Explain the difference between a proto-oncogene and a tumor suppressor gene.<\/li>\n<li>List the regulatory mechanisms that might be lost in a cell producing faulty p53.<\/li>\n<li>p53 can trigger apoptosis if certain cell cycle events fail. How does this regulatory outcome benefit a multicellular organism?<\/li>\n<\/ol>\n<\/div>\n<div class=\"textbox exercises\">\n<h3>Answers<\/h3>\n<ol>\n<li>A proto-oncogene is a segment of DNA that codes for one of the positive cell cycle regulators. If that gene becomes mutated, it is considered an oncogene. A tumor suppressor gene is a segment of DNA that codes for one of the negative cell cycle regulators. If that gene becomes mutated then the protein product becomes less active and the cell cycle will run unchecked. A single oncogene can initiate abnormal cell divisions.\u00a0 Tumor suppressors lose their effectiveness only when both copies of the gene are damaged.<\/li>\n<li>Regulatory mechanisms that might be lost include monitoring of the quality of the genomic DNA, recruiting of repair enzymes, and the triggering of apoptosis.<\/li>\n<li>If a cell has damaged DNA, the likelihood of producing faulty proteins increases. The daughter cells would produce faulty proteins that might eventually become cancerous. If p53 recognizes this damage, it triggers the cell to self-destruct, the damaged DNA is degraded and recycled. No further harm comes to the organism.<\/li>\n<\/ol>\n<\/div>\n<div class=\"textbox key-takeaways\">\n<h3>Glossary<\/h3>\n<p><strong>oncogene: <\/strong>mutated version of a normal gene involved in the positive regulation of the cell cycle<\/p>\n<p><strong>proto-oncogene: <\/strong>normal gene that when mutated becomes an oncogene<\/p>\n<p><strong>tumor suppressor gene: <\/strong>segment of DNA that codes for regulator proteins that prevent the cell from undergoing uncontrolled division<\/p>\n<\/div>\n\n\t\t\t <section class=\"citations-section\" role=\"contentinfo\">\n\t\t\t <h3>Candela Citations<\/h3>\n\t\t\t\t\t <div>\n\t\t\t\t\t\t <div id=\"citation-list-198\">\n\t\t\t\t\t\t\t <div class=\"licensing\"><div class=\"license-attribution-dropdown-subheading\">CC licensed content, Shared previously<\/div><ul class=\"citation-list\"><li>Biology. <strong>Authored by<\/strong>: Open Stax. <strong>Located at<\/strong>: <a target=\"_blank\" href=\"http:\/\/cnx.org\/contents\/185cbf87-c72e-48f5-b51e-f14f21b5eabd@9.17:1\/Biology\">http:\/\/cnx.org\/contents\/185cbf87-c72e-48f5-b51e-f14f21b5eabd@9.17:1\/Biology<\/a>. <strong>License<\/strong>: <em><a target=\"_blank\" rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\">CC BY: Attribution<\/a><\/em><\/li><\/ul><\/div>\n\t\t\t\t\t\t <\/div>\n\t\t\t\t\t <\/div>\n\t\t\t <\/section>","protected":false},"author":18,"menu_order":14,"template":"","meta":{"_candela_citation":"[{\"type\":\"cc\",\"description\":\"Biology\",\"author\":\"Open Stax\",\"organization\":\"\",\"url\":\"http:\/\/cnx.org\/contents\/185cbf87-c72e-48f5-b51e-f14f21b5eabd@9.17:1\/Biology\",\"project\":\"\",\"license\":\"cc-by\",\"license_terms\":\"\"}]","CANDELA_OUTCOMES_GUID":"","pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":[],"pb_section_license":""},"chapter-type":[],"contributor":[],"license":[],"class_list":["post-198","chapter","type-chapter","status-publish","hentry"],"part":179,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/pressbooks\/v2\/chapters\/198","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/wp\/v2\/users\/18"}],"version-history":[{"count":17,"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/pressbooks\/v2\/chapters\/198\/revisions"}],"predecessor-version":[{"id":1647,"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/pressbooks\/v2\/chapters\/198\/revisions\/1647"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/pressbooks\/v2\/parts\/179"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/pressbooks\/v2\/chapters\/198\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/wp\/v2\/media?parent=198"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/pressbooks\/v2\/chapter-type?post=198"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/wp\/v2\/contributor?post=198"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/nemcc-biology1v2\/wp-json\/wp\/v2\/license?post=198"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}