{"id":606435,"date":"2024-06-05T01:41:00","date_gmt":"2024-06-05T05:41:00","guid":{"rendered":"https:\/\/platohealth.ai\/reversible-molecular-changes-can-cause-cancer-study-shows\/"},"modified":"2024-06-05T09:15:31","modified_gmt":"2024-06-05T13:15:31","slug":"reversible-molecular-changes-can-cause-cancer-study-shows","status":"publish","type":"post","link":"https:\/\/platohealth.ai\/reversible-molecular-changes-can-cause-cancer-study-shows\/","title":{"rendered":"Reversible Molecular Changes Can Cause Cancer, Study Shows","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"

Reversible Molecular Changes Can Cause Cancer, Study Shows<\/a><\/h3>\n

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\n\t\t\t\t\t\t\t\tPosted on June 5, 2024<\/a><\/span> Updated on June 2, 2024<\/a><\/span>\t\t\t<\/span>\n\t\t<\/p>\n

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Though one in two people<\/a> will develop some form of cancer<\/a> in their lifetime, there\u2019s still much we don\u2019t know about this disease. But thanks to continued research efforts, we keep learning more about the biology of cancer. One of these recent discoveries could even transform our understanding of how cancers develop<\/a>.<\/p>\n

But before we talk about the new discovery, let\u2019s first discuss the classical theory that attempts to explain why normal cells become cancer cells. This theory posits that DNA mutations are the primary cause of cancers.<\/p>\n

It\u2019s well known that ageing, as well as some lifestyle and environmental factors (such as smoking and UV radiation) cause random DNA mutations (also known as genetic alterations) in our cells. Most genetic alterations trigger cell death or have no consequence.<\/p>\n

However, a few mutations favour cell survival. If a sufficient number of \u201clife extending\u201d DNA mutations occur in a cell, this cell will become virtually immortal \u2013 starting a series of uncontrolled duplications that generate a cancer. This theory has been corroborated by extensive experimental evidence<\/a>.<\/p>\n

However, this theory places a lot of importance on DNA mutations, which are irreversible<\/a> and often difficult to target<\/a> with drugs. So if cancer is caused by genetic mutations only, our ability to kill cancer cells may be limited.<\/p>\n

Interestingly, there are other theories on how cancer starts. If these theories are also valid, we could develop better ways of preventing and treating cancers.<\/p>\n

One of these new theories has been tested by researchers in a recent Nature publication<\/a>. This study was conducted in fruit flies (which share 75% of the genes<\/a> associated with human diseases).<\/p>\n

The researchers used the flies to investigate whether cancers could be caused by epigenetic changes<\/a> \u2013 reversible \u201cmarks\u201d that are added to the genome to turn genes on and off.<\/p>\n

\u201cGenetics\u201d and \u201d epigenetics<\/a>\u201d may sound similar, but they denote two very different processes. To understand the difference between genetic mutations and epigenetic alterations, think of your DNA as a book that contains some of the information needed to make yourself.<\/p>\n

According to this metaphor, each gene would be the equivalent of a sentence in this book. A genetic mutation would correspond to using a pen to scratch out or modify a sentence. Once done, you cannot undo it.<\/p>\n

Epigenetic marks are more subtle changes \u2013 like underlining a sentence with a pencil or using a bookmark to quickly retrieve a certain page. These changes are achieved by adding or removing small molecules to the DNA itself, or to the proteins that are closely associated to DNA.<\/p>\n

As such, epigenetic changes are reversible \u2013 but they can have a profound impact on the way your cells \u201cread\u201d the DNA.<\/p>\n

Epigenetic marks are essential for turning genes on and off during development (such as helping us form our eyes<\/a> in the womb). Epigenetic marks also create a bridge between the external environment and the genes. For example, epigenetic regulation of genes allows animals to adapt to changing seasons<\/a>.<\/p>\n

For a long time, epigenetic marks were considered too fleeting to actually cause cancer. But previous work by our research group and many others have shown that cancer cells accumulate several epigenetic alterations<\/a> \u2013 and these alterations can promote cancer cell survival as effectively as DNA mutations do.<\/p>\n

This would suggest that cancer develops through the accumulation of both genetic and epigenetic alterations.<\/p>\n

However, previous studies in this area hadn\u2019t had sufficient evidence to demonstrate epigenetic alterations could cause cancer in the absence of DNA mutations.<\/p>\n

This recent Nature study has shown for the first time that a temporary change in epigenetic marks \u2013 even without a DNA mutation \u2013 is sufficient to cause cancer.<\/p>\n

Treating cancer<\/h2>\n

This is not only a scientifically fascinating result, but evidence that could change the way we treat some cancers \u2013 especially if these results are confirmed in future studies.<\/p>\n

If epigenetic alterations contribute to cancer then researchers could develop epigenetic therapies for this deadly disease. Many scientists and pharmaceutical companies have been working on this<\/a> for the last few decades.<\/p>\n

These therapies would reprogram cancer cells by changing the distribution of reversible epigenetic marks. This would allow cells to revert to their normal behaviour, thereby stopping uncontrolled reproduction.<\/p>\n

Some of these new epigenetic drugs are now approved in some countries for the treatment of blood cancers and sarcomas<\/a>. Other epigenetic drugs are in clinical trials<\/a> for the most common cancer types \u2013 including breast and prostate cancer.<\/p>\n

The epigenetic cancer theory also has implications for cancer detection. Traces of abnormal epigenetic marks are released by cancer cells and can be found in the blood of cancer patients.<\/p>\n

This is why my colleagues and I<\/a> have described a blood test<\/a> that can detect epigenetic marks from tiny amounts of blood. Since DNA mutations can also be found in the blood of cancer patients, combining genetic and epigenetic tests could make cancer detection even more accurate.<\/p>\n

Epigenetic therapies can also be combined with traditional cancer therapies \u2013 such as surgery or radiotherapy, which are very effective in many cases.<\/p>\n

Our team also proposed that epigenetic drugs and tests<\/a> could potentially be used to develop better, more precise treatments that are optimised for each patient \u2013 though this technology is still a long way off.<\/p>\n

While the epigenetic theory of cancer explains important aspects of how the disease progresses, this doesn\u2019t mean the classical theory of cancer is wrong. This new theory enriches our understanding of a complex phenomenon, reminding us there\u2019s still a lot to learn about cancer.<\/p>\n

The next steps in this research are to test the epigenetic theory in other models \u2013 such as human cells \u2013 to further the development of precision treatments.<\/p>\n

Francesco Crea<\/a>, Senior Lecturer in Cancer Genetics, The Open University<\/a><\/em><\/p>\n

This article is republished from The Conversation<\/a> under a Creative Commons license. Read the original article<\/a>.<\/strong><\/p>\n

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