why the next great revolution against cancer is to make it chronic

If we ask someone what the goal of cancer medicine is, the answer is almost automatic: cure itmake it disappear or win the war against this devastating disease. However, in molecular biology laboratories and advanced oncology consultations, the verb is changing, since we no longer speak of “eradicating” at all costs, but to contain. An idea that may be quite shocking, but which is proposed as the future of medicine. The idea. Douglas Hanahan, one of the most influential figures in modern biology and one of the great responsible of the hallmarks of cancerwhich are the hallmarks that define a tumor, has put this idea on the table. In this case, it points to a concept that clashes with our intuition, but fits with scientific data: cancer without disease. The idea is provocative, since it suggests that histologically malignant tumors are possible living off of us without killing us or affecting our quality of life. The objective is no longer the total elimination of the enemy and becomes something more pragmatic: keeping it under biological and clinical control so that the patient dies with the cancer, but not from the cancer. There is no cure. In a recent interview and in your updates of the Hallmarks of Cancer 2022, Hanahan insists that the complexity of cancer makes a universal cure unlikely. Instead, it proposes to understand what specific capacities sustain the tumor, such as evasion of the immune system, inflammation, replicative immortality… to selectively block them. In this way, it is not about destroying the entire tissue, but about converting a lethal process into an indolent one. This is what Hanahan calls “adaptive resistance”, since we assume that the tumor will try to look for new escape routes, and we will change the therapeutic strategy to block them, maintaining the tumor ecosystem within safety margins. It already happens. All of this is not a futuristic theory, but rather it is already happening on two very different fronts: the tumors that we decide not to touch and the aggressive tumors that we have learned to stop. Not trying is sometimes the best. The most literal example of “cancer without disease” is found in the prostate and thyroid. Here, diagnostic technology has advanced so much that we detect tumors that, biologically, would never have caused problems. In the case of prostate canceralmost half of low-risk tumors now enter active surveillance protocols. In this way, instead of operating or radiating (with the risk of impotence and incontinence that entails), doctors begin to monitor the mass. And the data, after 20 years of follow-up in large groups of people, are quite clear: cancer-specific mortality in these well-selected groups is less than 1%. In the clinic. With all this, the idea is that it is better to live with a controlled cancer than to pay the physical price of curing it, although logically, if it goes too far out of containment, the most correct thing is to try to eradicate it with the tools we have. In the case of papillary thyroid cancer We also have this same situation, since overdiagnosis has led to stopping aggressive surgery in favor of observing tumors that the body keeps at bay on its own. The new chronicity. Where the paradigm changes most dramatically is in advanced or metastatic cancer. Twenty years ago, a diagnosis of stage IV lung cancer or metastatic melanoma was almost invariably a short-term terminal sentence. Today, thanks to immunotherapy and targeted therapies, a new category of patient has been born: the “treatable but not curable.” With this strategy there are already different organizations, like the British NCRIwhich describe growing cohorts of patients living for years with the disease. In this case they have metastases, but they live a normal life with their jobs and trips while receiving chronic or intermittent treatments to contain the disease. But without staying on the road. Changing the rules. This new paradigm within oncology has forced changing the rules of the game in clinical trialssince the aim is no longer just for the tumor to disappear, but for prolonged stabilization. With regard to toxicity, the logic of “maximum tolerated dose” in chemotherapy (give medication until the patient can tolerate it) does not work if you are going to treat the patient for five years, since their quality of life with very aggressive chemotherapy will decrease each time. Right now, quality of life and low toxicity are prioritized with ‘milder’ medications to allow long-term treatment without major side effects. This is why cancer is beginning to resemble, in its management, diabetes or HIV: a chronic condition that requires lifelong medication, but that does not necessarily dictate the date of your death. Psychological problems. Logically, this model of ‘chronic cancer’ has its shadows. Medical literature warns, for example, that living with “dormant” or controlled cancer places an enormous mental burden on patients. Studies on active surveillance show that, for some patients, the anxiety of having a “ticking time bomb” inside worsens their quality of life more than the surgery itself. And each review consultation can mean a world to know if it has gone more or less. And more problems. In addition to this, you must know that not all of these diseases can become chronic, such as glioblastoma or pancreatic cancer, which continue to have an aggressive biology that, today, escapes this lazy control. But also, turning cancer into chronic is great news for the patient, but a titanic challenge for public health, since it implies treating more people, for more years, with very high-cost biological drugs. The summary. Hanahan’s “cancer without disease” is not giving up. It is accepting that, if we cannot eliminate the enemy, victory lies in keeping it at bay long enough for life to continue its course and even allow science to continue advancing. As mortality statistics suggest: more and more people are dying with cancer, but fewer people of cancer. And in that nuance lies an entire medical revolution. Images | National Cancer … Read more

A massive study links it with a higher risk of chronic pain in adult

During generations, the message has been the same: menstrual pain is normal, a “girls” to endure. But the reality is that a pain of great draft never It is something that should have been normalized. Now, a Longitudinal study Published in The Lancet Regional Health – Europe comes to disassemble this myth and to give an alarm voice: Have painful periods In adolescence it is linked to health problems in the future. A public health problem. The methodology of this study has been based on the monitoring of more than a thousand participants in the United Kingdom for decades. In this way, not only has it been confirmed, it has been concluded that the more severe the menstrual pain at age 15, the greater the probability of developing chronic pain a decade later, at 26. In this way, menstrual pain goes from being normalized to a serious public health problem. A methodology with long -term views. To get to this conclusion, the researchers They used data of the Longitudinal Avon Study of Parents and Children (ALSPAC), An ambitious project that has followed the lives of thousands of people since birth in the 90s. They analyzed the information of 1,157 participants, evaluating the severity of their menstrual pain at 15 years classified as null, mild, moderate or severe. Subsequently, once these participants were already 26 years old, an analysis of their health status was carried out by asking if They suffered some kind of chronic pain. Something that was defined as a pain that lasted at least three months. Worrying figures. After adjusting the data to rule out the influence of other factors such as BMIthe socioeconomic level or previous mental health problems, the results were clear. The first of all, is that adolescents with moderate dysmenorrhea, that is, with strong enough pain to not be able to ignore it, they had an extra 65% probability of suffering chronic pain in the adult stage compared to those without menstrual pain. In the case of the most severe dysmenorrhea, which prevent normal activities, the risk is triggered up to 76% of suffering chronic pain in the future. These data translate into an increase in absolute risk of 12.7 and 16.2 percentage points, respectively. It is a difference too big to be ignored. The study also revealed how common this problem is: almost 60% of adolescents in the sample reported moderate to severe menstrual pain. A problem that extends through the body. One of the most interesting findings in the study is that the association is not limited to the classic abdominal or lumbar pain, which could be considered an extension menstrual pain. What happens in this case is that adolescents with severe dysmenorrhea show a greater risk of chronic head pain, back, knees, dolls, hips and thighs. Because? The authors of the study suggest that behind all this is a central sensitivity. To understand it, we must bear in mind that in adolescence there is a great neuroplasticity, where the nervous system is especially moldable. The repeated experience of intense and poorly managed pain, such as dysmenorrhea, can “train” the nervous system so that it becomes hypersensitive. In essence, the brain and spinal cord learns to be in a constant alert state, which increases vulnerability to develop other types of pain in the future, even in those areas that are not at all related. For Dr. Rachel Reid-McCann, principal researcher, “It is possible that the experience of moderate or severe menstrual pain can alter the structure of the brain and how it works in response to painful stimuli, making chronic pain more likely in the future.”. It is not a purely psychological. In the study itself, researchers have seen a relationship between dysmenorrhea and a subsequent increased symptoms related to anxiety and depression. But these factors only explained a small part of the connection with chronic pain and this reinforces the idea that the main cause is a physiological mechanism, and not simply that “pain is in the head.” You have to stop normalizing pain. The conclusion of the study is a call to action for father, educators and, above all, for the health system. Normalize menstrual pain and dispatch it as “is normal” has great long -term consequences. And that will go to the health system. The researchers point out that menstrual stigma and the lack of education on menstrual health cause many young people not to seek help, or that when they do, their complaints are minimized. In this way, it is believed that early identification and good control of dysmenorrhea can be key to improving the immediate well -being of adolescents and preventing the appearance of serious health problems in the future. Images | Saranya7 In Xataka | A baby, three parents (biological): a promising fertilization technique that, for now, we will not see in Spain

We have detected the gene that acts as a ‘switch’ of chronic pain. It is the principle of the analgesics revolution

Chronic pain is one of the worst convictions of modern medicine. Affects one in five peopleis the main cause of world dependence And to top it off, Current treatments They are insufficient or come with devastating side effects such as Opioid addiction as fentanyl. But now, A great investigation Posted in the prestigious magazine Nature It has opened a door that could change everything. A gene as responsible for chronic pain. An international team of scientists has identified a gene, the SLC45A4as a key actor in the perception of pain by the human. And it is not another gene on the list. They are the necessary instructions to manufacture a protein that acts as a “guardian” of the membrane of Our sensory neuronscontrolling the passage of mysterious molecules called polyamines. When manipulating this protein, researchers have reduced the intensity of certain pain without affecting other sensations such as The touch. The finding not only solves an old biological enigma, but also opens the door to a new generation of analgesics for patients with pains that are not controlled with current therapies. Following the track in the DNA of 130,000 people. Find a small gene Inside the human genome It is not something simple, taking into account the large amount of information that can be found In a sequencing. That is why researchers have resorted to brute force with the processing of a large amount of data. To do this, they analyzed the genetic information and pain questionnaires of more than 132,000 people from the UK Biobankone of the world’s greatest repositories of medical and genetic information. Looking for patterns in all data. Using a Complete genome association study (GWAS), which is like crossing thousands of data to find patterns, researchers discovered that certain variants of the SLC45A4 gene were significantly associated with the intensity of chronic pain that people reported. Something that could also explain the different pain thresholds that each person has. To ensure that it was not a coincidence, they replied the finding in two other gigantic databases such as the Million Veteran Program from the United States and Finngen of Finland. The result in both was similar, so the evidence began to clarify. But once you have the name of the gene, the question is: what exactly does this gene do to modulate pain? The guardian of the polyamines: solving a neuronal enigma. This is where history becomes very interesting. It was known that the SLC45A4 manufactured a conveyor protein, a kind of rotating door on the surface of the cells. But nobody knew what he transported. The investigation revealed that its load is the Polyaminessmall molecules that, despite being crucial for almost everything in the cell (From the reading of the DNA to growth), they had a role that was not known in pain. What was known is that during a pain situation polyamines increased, but the mechanism of action was a mystery. The reason for the mystery is that the effect was different depending on whether they were outside or inside the neuron, but the ‘door’ was not known through which they could enter or leave. Until now. The SLC45A4 protein is that door. Using advanced verification techniques. Before announcing a discovery like this, it is important to be verified with different techniques. In this case the Electronic Creomicroscopy To obtain a 3D map at the atomic level of the protein. In this way, they saw their structure with an amazing detail. But seeing it is not just to have a very beautiful photograph hanging in the office, but it could be understood how it was able to recognize polyamines and even a Modulable domain That the protein itself uses to inhibit itself, as an integrated key in its own lock. And this is something that opens many doors to future research related to chronic pain. Mice with the lowest pain threshold. The fire test came with the experiments in animals. The team created genetically modified mice so that they did not have the SLC45A4 gene. These mice were, in appearance, completely normal. However, when they were subjected to pain proof, the results were amazing. Specifically, mice were subjected to different tests, such as being on a hot plate or receiving a formalin injection, which is a chemical that Causes pain at high doses. Here it is as they showed a much greater resistance to chronic pain. But when they were given a quick puncture (acute pain) the answer was identical to that of normal mice. A pain regulator. And this difference is crucial in the investigation. It means that SLC45A4 is not a switch that when we go out ‘we stop feeling any type of pain, but is a fine regulator for persistent and deaf pain, precisely the type that characterizes chronic pain. Because living completely without pain is not a good idea. The pain in the end is an organism alert system that something is not doing well, for example, that we have appendicitis. If we ‘turn off’ acute pain are many emergency situations that we would literally stop attending until it was too late. And reason is known. The absence of the protein made a specific type of pain receptors, the so -called Polymodal nociceptors C or fibers C (Those that detect chemical or thermal pain), were much less excitable. That is, it was necessary to expose the receiver to a much stronger stimulus so that the neurons ‘trigger’ an action potential that reached the brain and gave the feeling of pain. Literally, the threshold potential was much lower and, therefore, resisted from great magnitude pain. A new hope for millions of people. This discovery is more than a simple scientific curiosity. By identifying this protein as the polyamine transporter in neurons related to nociception, a completely new window for drug design opens. And it is that current analgesics act on receptors or block (such as the case of ibuprofen with COX-2). Now, the drugs designed to modulate the activity of … Read more

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