Tuesday, January 07, 2020

Researchers study new immunogenic properties of already existing anti-cancer drugs

The world scientific community is waging a difficult and prolonged war on cancer. New research in the field of immunogenic cell death can extend the area of drugs application and ensure patients' protection from relapse after therapy.

Cancer treatment is not just the removal of the tumor cells from the body, and chemotherapy. The doctors' aim is to provide a scenario that would prevent tumor cells from proliferating and causing a new disease.

For many years, scientists at the Lobachevsky State University of Nizhny Novgorod and the University of Ghent (Belgium) have been engaged in research aimed to minimize the harm to the body after cancer treatment and have been looking for new approaches to treating cancer patients. 

The project, supported by a grant from the Russian Science Foundation and headed by Dmitry Krys'ko, leading researcher of the Lobachevsky University's Institute of Biology and Biomedicine, professor at Ghent University, has yielded its first major results.

According to Professor Dmitry Krys'ko, the existing anti-cancer therapy (chemotherapy, radiation therapy and photodynamic therapy) causes great damage to the body as a whole, while his team's research is aimed at the stimulation of immunogenic cell death, which not only minimizes the damage, but also enhances the efficacy of treatment by involving the body's resources in the fight against cancer.

In this study, we tested some drugs for anticancer therapy based on photodynamic treatment and investigated their new immunogenic properties. We can say that not only the external impact will be used to fight cancer, but also the body itself will engage in the fight by triggering the reactions of the adaptive immune response.

The concept of immunogenic cell death (ICD) includes a programmed death of cancer cells with subsequent release of molecules that give a danger signal to the immune system. We tested the drugs that are already used in cancer therapy, and enhanced the action of these agents."

Dmitry Krys'ko, leading researcher of the Lobachevsky University's Institute of Biology and Biomedicine, professor at Ghent University

The study employed a number of methods and approaches that were used in in vitro and in vivo experiments. At the laboratories of Lobachevsky University and the University of Ghent, researchers studied how substances accumulate in the cell, analyzed cell death types when cells were exposed to photosensitizers, and revealed molecular mechanisms of the phenomena that occur to the cells in the process of their death.

"In this study, we examined the cellular-level response of dendritic cells (immune system components) in their interaction with cancer cells that were exposed to photodynamic therapy (PDT) and proved that photodynamic therapy can activate the body's own immune response," said Victoria Turubanova, research assistant of the Department of General and Medical Genetics at the UNN Institute of Biology and Biomedicine.

The researchers have examined additional aspects of the use of existing drugs for developing new cancer protocols based on the stimulation of the immune system. Such variants of therapy reduce the risk of metastasis and enhance the effectiveness of the patient's recovery.

A series of experiments on laboratory mice was performed, resulting in an important conclusion that the cellular vaccine prepared from dying cancer cells protects the mouse from cancer by preventing tumor development in the body.

Based on the results obtained, the researchers have published their article "Immunogenic cell death induced by a new photodynamic therapy based on Photosens and Photodithazine" in the BMC Journal for ImmunoTherapy of Cancer (with the impact factor of 8.67), which describes new variants of photosensitizers that cause immunogenic cell death of cancer cells.

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Monday, March 18, 2019

Coffee compounds may help to reduce prostate cancer risk

Scientists have identified kahweol acetate and cafestol hydrocarbon compounds naturally found in Arabica coffee which may inhibit the growth of prostate cancer.

The pilot study showed kahweol acetate and cafestol can inhibit growth in cells that are resistant to common anti-cancer drugs like Cabazitaxel.

“We found that kahweol acetate and cafestol inhibited the growth of cancer cells in mice, but the combination seemed to work synergistically, leading to a significantly slower tumour growth than in untreated mice,” said lead author.

For the study, presented at the European Association of Urology Congress in Barcelona, the team tested six compounds, naturally found in coffee, on proliferation of human prostate cancers cells in vitro (i.e. in a petri-dish).

They found cells treated with kahweol acetate and cafestol grew more slowly than controls. They then tested these compounds on prostate cancer cells, transplanted to mice (16 mice).

“After 11 days, the untreated tumours had grown by around three and a half times the original volume (342 per cent), whereas tumours in the mice treated with both compounds had grown by just over one and a half (167 per cent) times the original size,” he said.

It also showed the growth reduction occurred in transplanted tumour cells, rather than in native tumour cells.

Although “these are promising findings, but they should not make people change their coffee consumption,” cautioned Professor from the varsity.

“Coffee can have both positive and negative effects. We need to find out more about the mechanisms behind these findings before we can think about clinical applications. But if we can confirm these results, we may have candidates to treat drug-resistant prostate cancer,” he noted.


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Saturday, April 07, 2018

Most anti-cancer drugs can affect the cardiac pumping function

Cancer therapy has been at receiving end for quite some time now. A few years ago, a British doctor shot to fame when he refused to accept modern medicare for his cancer treatment. He opted to die of cancer than suffer from the adverse effects of its therapy. Recently, a lady who claimed to have found a cure for cancer in fruits and vegetables died of cancer, too. A film actor and director managed to stall a government proposal to start a cancer center in central Kerala, out of his conviction that modern medicine has no cure for cancer and cancer drugs if dumped is capable of killing the entire fish population of the Arabian Sea. Not just that, someone even put a fake post in the name of a celebrated oncologist on Facebook promoting alternative therapy for cancer, which was then shared widely. 

Why is cancer treatment alone is singled out by the public and lamented at? Why do those who have no basic training in medicine call the shots in cancer care? Why are oncologists and others involved in cancer care taken for granted as agents of multinational drug firms trying to sell expensive concoctions to unsuspecting cancer victims?

Statistics tell us that cancer survival rate has improved by over sixty per cent during the last 40 years, owing to advances in chemotherapy, oncosurgery, radiation, oncology, imaging sciences and other supportive specialties including oncocardiology. Cancers like nasopharyngeal cancer, pancreatic cancer and cancers among young adults have less impressive cure rates. Breast and prostate cancer are curable. These patients when diagnosed and treated appropriately, do not die of cancer, but of other illnesses. Evidence-based medicine has proved beyond doubt that alternative therapies and nature cure is not effective for treatment of cancer.

Why do people expect a cure for cancer like a common cold, malaria, or an infective diarhoea? Anti-cancer drugs have significant side effects and sensitive dose ranges. Most anticancer drugs can potentially affect the heart, especially cardiac pumping function leading to heart failure. Some can cause elevation of blood pressure, cardiac rhythm abnormalities, heart attacks, venous thromboembolism and even new cancers. Reports show that immunotherapy too can cause fulminant heart failure. 

A pertinent question arises here. If these medications cause such damage, why they should ever be used? Reason: They cure cancer. We see more and more people with adverse effects because patients survive cancer and live longer. If they were dead, you won’t get to see adverse events too. More patients are alive with cancer, so you see more relics of cancer.As life expectancy improves, and population survives infectious diseases out of better living standards, antibiotics, vaccination and social engineering, lifestyle disorders and cardiovascular disease by improvement in physical activities, diet modifications, medications, other interventions and conquer death out of it, then it is a biological plausibility that most of us will catch cancer or degenerative disorders in due course of time. Unlike many doomsayers scream, life expectancy is improving all over the globe, including in some of the most underprivileged societies.

This is a reality. When population ages, natural conditions like cardiac illnesses, cancer, kidney failure and degenerative diseases will be on the rise.We will have to live with all of these maladies. Scientific approach to issues are critical and government policies will be crucial. Radical changes in health care delivery systems will become the need of the hour, hospices will become more relevant that can accommodate and care for people who need attention, short of hospitalisation. We will have to promote research; improve social infrastructure, public conveyances, and social security. That is the way population will live longer, healthier and better. 

Can you imagine even someone like Steve Jobs was a fan of alternate therapies for cancer and died out of an eminently treatable form of cancer of the pancreas denying us more advanced iPhones, iMacs, and iscreens?

The author is an Interventional Cardiologist, with a special interest in cardiac involvement in cancer therapies. He was a fellow in cancer biology and therapeutics.

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Wednesday, November 23, 2016

Drinking green tea may ease kidney damage caused by anti-cancer drug

Green tea is effective in reducing the kidney toxicity and damage caused by cisplatin -- an anti-cancer drug, the AIIMS researchers have revealed.

The research study has evaluated the usefulness of ECG, a polyphenolic compound obtained from green tea in preventing the damage of kidneys induced by the cisplatin. Side effects of cisplatin may include nephrotoxicity and life-threatening damaged kidney.

The study by AIIMS Professor Jagriti Bhatia from the Pharmacology Department was published in journal 'Laboratory Investigations' recently.

"If this research progresses, it may lead to a new drug which can combat the ill effects of cisplatin," said Bhatia.

Approximately, 30 per cent of the treated patients may develop nephrotoxicity after receiving an initial dose of cisplatin. Cisplatin causes production of free radicals inside cells in kidney which leads to oxidative stress and inflammation.


this is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.

https://gscrochetdesigns.blogspot.com. one can see my crochet creations
https://gseasyrecipes.blogspot.com. feel free to view for easy, simple and healthy recipes

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Green tea is effective in reducing the kidney toxicity and damage caused by cisplatin -- an anti-cancer drug, the AIIMS researchers have revealed.

The research study has evaluated the usefulness of ECG, a polyphenolic compound obtained from green tea in preventing the damage of kidneys induced by the cisplatin. Side effects of cisplatin may include nephrotoxicity and life-threatening damaged kidney.

The study by AIIMS Professor Jagriti Bhatia from the Pharmacology Depa ..

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Saturday, October 17, 2015

Malaria protein could help treat cancer

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 The mosquito-borne parasite that causes malaria also produces a protein that could help stop cancer, new research has found.

The researchers found that the malarial protein binds to a sugar molecule found in many types of cancer.

The sugar molecule -- oncofetal chondroitin sulfate -- could be a target for anti-cancer drugs, and that the malarial protein, called VAR2CSA, could provide the tool for carrying such drugs to tumours, the scientists found.

"Based on our clinical data, we helped validate that this could be applied to melanoma and lung cancers," said one of the authors of the study Nhan Tran, associate professor at Translational Genomics Research Institute (Tgen) in Arizona, US.

"This specific type of developmental protein -- oncofetal chondroitin sulfate -- is expressed in the placenta, and is also expressed in lung cancer and in melanoma," Tran said.

Malaria uses VAR2CSA to embed itself in the placenta -- hiding itself from the immune system -- by binding to oncofetal chondroitin sulfate.

In laboratory experiments, researchers found that if they used the malarial protein, VAR2CSA, and attached an anti-cancer drug to it, it would bind with the oncofetal protein in the cancer, delivering the drug to the tumour.

The study was published in the journal Cancer Cell.

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