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<p class="publishdate"><span property="dc:date" datatype="xsd:dateTime" content="2021-03-30T00:00:00-04:00" class="date-display-single">March 30, 2021</span></p><div class='syndicate'><h1>Gene therapy for chronic pain relief</h1><div class="callout callout-with-border"><h3>At a Glance</h3>
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<ul>
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<li>Turning off a particular gene prevented or alleviated chronic pain in mice.</li>
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<li>The results could lead to an alternative to opioids for treating chronic pain.</li>
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</ul></div><div class="media-float-right"><div class="ds-1col file file-image file-image-jpeg view-mode-floated_media clearfix">
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<picture title="3D illustration of sensitized nerves">
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<!--[if IE 9]><video style="display: none;"><![endif]-->
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-large/public/news-events/research-matters/2021/20210330-fungi.jpg?itok=bAaXGhdp&timestamp=1617112018 1x" media="screen and (min-width: 960px)" />
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-medium/public/news-events/research-matters/2021/20210330-fungi.jpg?itok=CvnwROLx&timestamp=1617112018 1x" media="screen and (min-width: 800px)" />
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-medium-small/public/news-events/research-matters/2021/20210330-fungi.jpg?itok=A-ZD6Ye6&timestamp=1617112018 1x" media="screen and (min-width: 600px)" />
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-small/public/news-events/research-matters/2021/20210330-fungi.jpg?itok=nNLXmB0j&timestamp=1617112018 1x" media="screen and (min-width: 480px)" />
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-tiny/public/news-events/research-matters/2021/20210330-fungi.jpg?itok=_90-M7CT&timestamp=1617112018 1x" media="screen and (min-width: 0)" />
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<!--[if IE 9]></video><![endif]-->
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<img src="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-medium/public/news-events/research-matters/2021/20210330-fungi.jpg?itok=CvnwROLx&timestamp=1617112018" alt="3D illustration of sensitized nerves" title="3D illustration of sensitized nerves" />
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</picture><span class="caption">Researchers designed ways to dampen pain signals in nerves that are are sensitized, or more susceptible, to pain. </span><span class="credit">FlashMovie / iStock / Getty Images Plus</span></div>
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</div><p>Opioids remain the standard of care for many cases of chronic pain. While they are often the best option available, they also have drawbacks that make them less than ideal. These include adverse side effects and a tendency to make people more sensitive to pain over time, leading to a risk of addiction. Researchers have thus been looking for alternatives to relieve chronic pain.</p>
|
||
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||
<p>Proteins called voltage-gated sodium channels control pain sensation by regulating the flow of sodium ions into certain nerve cells. A genetic mutation that disables one of these proteins, called Na<sub>V</sub>1.7, renders people unable to feel physical pain (the human gene name is <em>SCN9A</em>). Na<sub>V</sub>1.7 thus makes a promising target for new pain-relieving drugs. Unfortunately, Na<sub>V</sub>1.7 is very similar to several other proteins. Researchers have been unable to develop a drug that can target Na<sub>V</sub>1.7 without affecting these related proteins.</p>
|
||
|
||
<p>A team led by Drs. Prashant Mali and Tony Yaksh at the University of California, San Diego, have developed an alternate method for inactivating Na<sub>V</sub>1.7: turning off the gene that encodes it.</p>
|
||
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||
<p>Their study was supported in part by NIH’s National Institute of Neurological Disorders and Stroke (NINDS), National Human Genome Research Institute (NHGRI), National Cancer Institute (NCI), and National Institute of General Medical Sciences (NIGMS). Results appeared on March 10, 2021 in <em>Science Translational Medicine.</em></p>
|
||
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||
<p>To turn off the Na<sub>V</sub>1.7 gene, the researchers used two approaches. One used a modified form of the CRISPR gene editing system. Normally, CRISPR relies on an enzyme called Cas9 to cut DNA at a specific sequence. Instead, the researchers used a “dead” Cas9 that can locate and bind to its target DNA sequence but can’t cut the DNA. They fused this dead Cas9 to a protein called a repressor, which blocks gene expression. This created a molecule that could turn off the gene without altering the DNA sequence.</p>
|
||
|
||
<p>They also used an older gene editing tool called zinc finger proteins. Like Cas9, these bind to specific DNA sequences. They were also fused to a repressor to turn off gene expression at the binding site. The researchers dubbed their strategy long-lasting analgesia via targeted in vivo epigenetic repression of Na<sub>V</sub>1.7. or LATER.</p>
|
||
|
||
<p>To test LATER, the researchers injected these constructs into the spinal canals of mice and treated their paws to make them more sensitive to pain. When exposed to heat, cold, or pressure, mice treated with either of the LATER constructs had higher pain thresholds than untreated mice. This pain relief lasted for several weeks. The full duration of pain relief is still unknown. Treated mice behaved normally and showed no apparent side effects.</p>
|
||
|
||
<p>The researchers believe that the LATER strategy has potential for managing chronic pain in people. They have founded a company called Navega Therapeutics to develop LATER into a clinical treatment. But further work is still needed before LATER will be ready for human trials. Production of Na<sub>V</sub>1.7 differs between mice and humans, so the system may need adjustments to work in people. And its efficacy and potential toxicity will need to be tested in non-human primates. But these results have given the researchers a promising start.</p>
|
||
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||
<p>“We were excited that both approaches worked,” Mali says. “The beauty about zinc finger proteins is that they are built on the scaffold of a human protein. The CRISPR system is a foreign protein that comes from bacteria, so it could cause an immune response. That’s why we explored zinc fingers as well, so we have an option that might be more translatable to the clinic.”</p>
|
||
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||
<p>—by Brian Doctrow, Ph.D.</p></div><h2 class="label-above">Related Links</h2><ul class="spaced print-urls"><li><a href="https://www.nih.gov/news-events/nih-research-matters/pain-rising-among-younger-americans-less-education" target="_top">Pain Rising Among Younger Americans with Less Education</a></li><li><a href="https://www.nih.gov/news-events/nih-research-matters/scientists-find-new-pain-suppression-center-brain" target="_top">Scientists Find New Pain-Suppression Center in the Brain </a></li><li><a href="https://www.nih.gov/news-events/nih-research-matters/how-gentle-touch-can-turn-painful-after-injury" target="_top">How Gentle Touch Can Turn Painful After Injury</a></li><li><a href="https://www.nih.gov/news-events/nih-research-matters/how-opioid-drugs-activate-receptors" target="_top">How Opioid Drugs Activate Receptors</a></li><li><a href="https://www.nih.gov/news-events/nih-research-matters/opioid-pain-relievers-may-prolong-pain" target="_top">Opioid Pain Relievers May Prolong Pain</a></li><li><a href="https://www.nih.gov/news-events/nih-research-matters/gene-affects-pain-sensitivity" target="_top">Gene Affects Pain Sensitivity</a></li><li><a href="https://newsinhealth.nih.gov/2018/10/managing-pain" target="_top">Managing Pain: Moving Beyond Opioids</a></li><li><a href="https://www.nccih.nih.gov/health/pain" target="_top">Pain</a></li><li><a href="https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Hope-Through-Research/Pain-Hope-Through-Research" target="_top">Pain: Hope Through Research</a></li><li><a href="https://www.drugabuse.gov/drug-topics/opioids" target="_top">Opioids</a></li></ul><p class="footnote"><strong class="label-inline">References: </strong><a href="https://pubmed.ncbi.nlm.nih.gov/33692134/">Long-lasting analgesia via targeted in situ repression of NaV1.7 in mice.</a> Moreno AM, Alemán F, Catroli GF, Hunt M, Hu M, Dailamy A, Pla A, Woller SA, Palmer N, Parekh U, McDonald D, Roberts AJ, Goodwill V, Dryden I, Hevner RF, Delay L, Gonçalves Dos Santos G, Yaksh TL, Mali P. <em>Sci Transl Med</em>. 2021 Mar 10;13(584):eaay9056. doi: 10.1126/scitranslmed.aay9056. PMID: 33692134.</p><p class="footnote"><strong class="label-inline">Funding: </strong>NIH’s National Human Genome Research Institute (NHGRI), National Cancer Institute (NCI), National Institute of General Medical Sciences (NIGMS), National Institute of Neurological Disorders and Stroke (NINDS), and Office of the Director (OD); University of California San Diego; Consejo Nacional de Ciencia y Tecnología; University of California Institute for Mexico and the United States; Fundação de Amparo à Pesquisa do Estado de São Paulo.</p>
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