Monday, February 23, 2015

Heart Health After Cancer: A Growing Concern

Nearly 15 million people are living after a cancer diagnosis in the United States. This number represent over 4 percent of the population, an astonishing figure. And a growing one, as reported last year by the ACS and outlined by the NCI’s Office of Cancer Survivorship.
As cancer patients survive longer they face additional health problems. Radiation to the chest, chemotherapy, antibody therapy and hormone changes can affect blood vessels and heart function in the short term and long, during treatment or years later. But millions affected – and their physicians – remain insufficiently mindful about the risk of heart disease.
It’s the kind of problem a person who’s had cancer, or a doctor who’s prescribed generally helpful treatment, may not want to think about.
Years ago, heart complications of cancer treatment didn’t garner so much attention says, Dr. Javid Moslehi, a cardiologist who leads a program in cardio-oncology at the Vanderbilt University School of Medicine in Nashville, TN. The emerging field involves cardiologists, oncologists, scientists and others who study the long-term effects of cancer treatment on the heart.
“In the past, people were just glad to be alive,” he said. “With so many survivors, there’s a growing need to understand how we can avoid toxic effects of treatment,” he said. “Cardiac issues are becoming central,” he said.
To promote heart health after cancer treatment, Moslehi and collaborators put forth an ABCDE plan that was published last year in Circulation. The “ABCDE” program, developed with a group including Dr. Ann Partridge at Boston’s Dana Farber Cancer Institute, lists pro-active steps a woman with breast cancer might take to prevent or lessen her chances of heart disease.
The ABCDE acronym is a bit more complicated than its five letters might suggest. The gist of the proposed program, published here, is this:
A is for Awareness of the risk of heart disease (and Aspirin, which some might take upon consultation with a doctor);

B is for Blood pressure – which might need monitoring;
C is for Cholesterol – to keep it low (and Cigarettes – to stop smoking, and your author’s preferred “C”);
D is for Diet – keeping your weight down is good for survival (and for Dose – whether it’s chemo or radiation, how much you get affects risk; and for Diabetes – averting it if possible, controlling it if you have the condition);
E is for Exercise – Do it! (if you’re able; and for Echocardiogram, this images how well the heart is functioning; it’s not a bad way to keep an eye on things if you’re on a drug, like Herceptin among others, that might need be stopped, or the dose adjusted).
The ABCDE take-away is that there are steps a cancer patient might take to deter heart disease. While this initial plan focuses on women who've had breast cancer, the largest cohort of survivors, the principles of preventing or minimizing cardiac problems might help those with other cancer types. Prospective studies are needed.
For the more than 3 million U.S. women who have had breast cancer, the possibility of heart damage from is quite real. Apart from heart disease from chemotherapy drugs and radiation, there may be an augmented risk after early menopause. Natural estrogens, which are deliberately blocked by some types of breast cancer treatment, may be cardio-protective – and were thought to explain why men are more prone to heart disease than women.
February is Heart Health Month. (image adapted, credit: Billie Ward via Flickr)
February is Heart Health Month. (image adapted, credit: Billie Ward via Flickr)
After breast cancer treatment, women should be mindful of heart disease symptoms, which can be subtle. The unfortunate reality is that many doctors, nurse practitioners and others fail to adequately consider the possibility of vascular and other diseases of the heart when evaluating healthy-seeming and non-elderly women.
So the need for greater awareness of risk applies to physicians, too, especially as patients may move or lose access to their oncologist who knows what they received years or decades earlier. Patients aren’t perfect, either; some “forget” or might not remember if they received radiation 25 years ago after a lumpectomy.
As new drugs become available, the side effects of each treatment, and combinations, should be more carefully weighed. “The FDA is becoming much more focused on cardiovascular safety of cancer drugs,” Moslehi said.
For instance, in October 2013 the FDA pulled back on approval of ponatinib (Iclusig, Ariad Pharmaceuticals), a drug used for treating CML, a chronic form of leukemia. The main reason for the FDA’s switch, which turned yet again after advocates and doctors pushed for continued access to the drug was concern over its vascular toxicity including effects on the heart.
“The CML drug was transiently taken off the market because it wasn’t deemed essential,” Moslehi said. But in some cases of CML, it turns out that ponatinib is the only drug that works. Now the drug is back on the market. But there’s little data on how to avoid its cardiac complications, he noted. Radiation has been a major culprit in accelerating heart disease, Moslehi said.
In recent decades, radiation oncologists have developed methods to protect the heart during treatment. It’s better now than it was in the 1980s and even the 1990s, he suggested. “It may be a greater problem for patients who received radiation a long time ago.”
Old chemotherapy drugs like Adriamycin (the “red devil”) and its chemical relatives are long-known for their capacity to harm a patient’s heart. Years ago, oncologists knew to order serial heart assessments before and after every few cycles of these drugs, to make sure the infusions were doing more good than harm.
The Google-able list of heart toxicity is scary, wide and long, enough to depress almost anyone who’s had treatment. If you look, you’ll find: Recent reports confirm the damaging potential of some of the earliest and most widely-used cancer medications, like 5-fluorourcacil (5-FU). Drugs like taxol can slow the heart and more. Cyclophosphamide delivers its own set of concerns, especially if it’s given at high doses. Herceptin, a drug that has transformed the prognosis (from bad to good) for countless patients, has well-documented cardiac toxicity.
The list goes on, but I’ll stop here. It’s enough to scare the wits out of a reader or person like me who’s trying to move forward with a healthy life after cancer treatment. The ways that cancer drugs cause heart damage are diverse, Moslehi said in an interview with the American College of Cardiology’s CardioSource. Old chemotherapies and radiation are toxic, but so are many newer drugs, he emphasized: angiogenesis inhibitors can cause high blood pressure and clots; tyrosine kinase inhibitors cause vascular disease; one class of agents, called HDAC inhibitors, cause abnormal heart rhythms; other drugs called mTOR inhibitors, lead to metabolic changes that affect the heart.
“It’s complicated,” he told me. “Unfortunately, we have very little idea of what the right assessment before, during and after treatment should be.”
“Anthracyclines are still used for Hodgkin’s, breast cancer and lymphoma. They have lots of cardiac toxicity,” Moslehi told me by phone. “In the past this was not an issue because there were no other therapies to give.”
He and other cardio-oncology investigators are studying the molecular changes that lead to heart problems after cancer. The goal is to find ways to predict and prevent heart disease in people who otherwise benefit from cancer drugs. Ideally the drugs and doses might be selected, or avoided, in each case with information about the patient’s tumor and cardiac risk.
“The whole reason we have this problem in the first place is that the treatments for cancer are so effective, Moslehi said. “The last thing we want to do is take away good treatments.”
–
To receive my articles, follow me here at Forbes.  I’m on Twitter @ElaineSchattner. For my public updates on Facebook hit the “follow” button.

Saturday, February 21, 2015

Olive oil ingredient leads cancer cells to their death

February 19, 2015
A compound in extra-virgin olive oil has been found to destroy cancer cells without harmin...
A compound in extra-virgin olive oil has been found to destroy cancer cells without harming healthy cells (Photo: Shutterstock)
An ingredient found in extra-virgin olive oil called oleocanthal has been known as a compound capable of killing a variety of human cancer cells, but how this process actually played out was not understood. Now, a team of researchers has uncovered not only how oleocanthal destroys cancer cells, but that it is able to do so while leaving healthy cells unharmed.
Paul Breslin, a professor of nutritional sciences at Rutgers University, had thought that oleocanthal killed the cancer cells by targeting a key protein in cancer cells that triggers apoptosis, a process that sees dangerous or damaged cells self-destruct by upsetting the balance of ions in the cell membranes. In investigating this theory, he teamed up with David Foster and Onica LeGendre, two cancer biologists from New York City's Hunter College to more closely examine the process.
"We needed to determine if oleocanthal was targeting that protein and causing the cells to die," says Breslin.
What first surprised the scientists was how quickly the oleocanthal destroyed the cancer cells. While apoptosis requires between 16 and 24 hours to take effect, the oleocanthal was killing off the cancer cells within 30 minutes to one hour. This led the team to believe that there were some other factors at play.
What they discovered was that the oleocanthal was piercing the cancer cell's vesicles, the containers that store the cell's waste. By puncturing these "dumpsters," as Breslin describes them, it creates an outpouring of enzymes that then cause the cell to die.
"Once you open one of those things, all hell breaks loose," says Breslin.
And when it came to the healthy cells, the researchers found that they remain completely unharmed. While the application of oleocanthal caused a temporary halt in their life cycles, after 24 hours they returned to normal.
With the testing thus far carried out in the lab, the researchers say that they will now look to establish the effects of oleocanthal on cancer cells in living animals.
The findings were published in the journal Molecular and Cellular Oncology.

Thursday, February 19, 2015

Cancer treatments could evolve from research showing that acetate supplements speed up cancer growth

UT Southwestern Medical Center researchers seeking novel ways to combat cancer found that giving acetate, a major compound produced in the gut by host bacteria, to mice sped up the growth and metastasis of tumors.
Bacteria living inside the gut can have beneficial, but potentially also harmful effects on human health. Further studies are needed to determine whether restricting acetate production by  will affect growth of tumors.
"With insights generated from our current studies, we may be able to design therapies that treat  patients by modulating acetate production in the body," said Dr. Joseph Garcia, Associate Professor of Internal Medicine at UT Southwestern and staff physician-scientist at the VA North Texas Health Care System.
The work is published in the February issue of the journal PLOS ONE.
Cancer, the second leading cause of death in the US, is estimated to account for nearly 1 out of every 4 deaths in 2014. It can have a significant impact on length and quality of life, which carries a tremendous economic burden. Cancer can develop in any part of the body and some are notoriously difficult to treat, although recent discoveries from basic science laboratories hold great promise for more effective treatments and potential cures.
In , low oxygen and low glucose conditions turn on signaling pathways that allow otherwise healthy cells to survive these stresses. UT Southwestern researchers previously discovered a critical pathway that controls the response of cells and organs to , a state known as hypoxia. In this study, the researchers show that the production of acetate is also stimulated by low glucose conditions, another condition frequently found in solid tumors.
Acetate, in turn, activates a molecular pathway that ultimately results in the production of several proteins that stimulate the growth and spread of tumors.
"Our study shows that acetate functions in this context as a growth signal for cancer cells, one that links changes in metabolism within cancer cells that occur during tumor growth with activation of a selective stress-. This same signaling pathway is normally protective in healthy individuals. In fact, stimulating this pathway in anemic mice without cancer has a profound effect on restoring red blood cell levels to near-normal or normal levels, and is otherwise very safe" said Dr. Garcia, a member of the Harold C. Simmons Comprehensive Cancer Center.
"The challenge facing us now is to define which patients may benefit from having this pathway stimulated and which patients will benefit from having this pathway inhibited. Preclinical studies of this nature are essential for informing the pharmaceutical and federal health oversight agencies about potential benefits as well as potential harms that may result from use of compounds that affect this key signaling pathway," said Dr. Garcia.

Chemobrain—It’s Real, It’s Complex, and the Science Is Still Evolving

Author: Susan Krigel, PhD

Talk with almost any cancer survivor, and he or she is likely to bring up the topic of “chemobrain,” that  that fuzzy, murky state that patients blame for impaired memory. When physicians first began hearing patients complain about chemobrain, they may have wondered whether it truly existed. As time has passed, they may now be wondering why science hasn’t found a solution.

A review of the research documenting cognitive decline after chemotherapy indicates that the most common complaints have concerned learning and memory, processing speed, verbal and spatial abilities and executive function (planning and decision-making).

Interestingly, about half of the studies reviewed documented cognitive decline even before the initiation of chemotherapy. Cognitive impairment due to chemotherapy can significantly impair a patient’s quality of life. A recent review of 17 qualitative studies focusing on patients’ experience of chemobrain documented that patients reported fearing that they “were going crazy,” or developing Alzheimer’s. Patients noted they had difficulty learning and had to work harder to accomplish tasks. As a result, they were less confident in work and social situations.

[Read "Finding Solutions for Chemobrain" from CURE's winter 2013 issue]

Estimates vary on the prevalence and duration of chemobrain, due in part to timing of assessment and degree of impairment. A recent meta-analysis demonstrated that about 16 percent to 75 percent of breast cancer patients had moderate to severe impairment. As may be expected, deficits are most evident during treatment, with most patients returning to baseline within a few months of completing chemotherapy. However, a subset of patients has been found to have ongoing deficits, even after 20 years. Older patients with lower cognitive reserve at baseline are most likely to have higher levels of impairment. Co-occuring factors may also contribute to chemobrain. Approximately 30 percent of cancer patients experience depression, anxiety or distress during treatment, and depressed individuals score lower than non-depressed individuals on neuropsychological tests in attention, sustained attention, processing speed, recall, fluency, and speed of retrieval.

Fatigue, an almost universal symptom during and shortly after cancer treatment, may impair memory by decreasing attention, processing speed, and motivation. In addition, about 30 percent to 60 percent of cancer patients report having insomnia, which may cause poor concentration and memory.

What Is the Evidence Behind Chemobrain?

Although cancer patients have been reporting symptoms of cognitive impairment for many years, the first scientific studies began appearing in the mid-1990s. Some of the first studies began exploring the impact of particular chemotherapy protocols on cognition.

But as studies progressed, it seemed that more questions arose than were being resolved. There were so many confounding factors, such as age, hormonal status, baseline cognitive performance, educational level, genetic predisposition, comorbidities that impact oxygenation, depression, anxiety, fatigue, pain, anemia, time since treatment and dietary factors. How would it be possible to control for all those factors?

Thankfully, advances in neuroimaging have provided us with information that has moved the field forward. Functional MRI (fMRI) studies have documented that: Chemotherapy results in both cerebral functional and structural changes; the alterations correlate with complaints regarding impaired cognition and performance, and the alterations persist over time.

In an early study exploring functional changes in the brain due to chemotherapy, researchers asked twin, 60-year-old females, one of whom had been treated with chemotherapy, to perform a series of tasks while undergoing fMRI. The resulting images documented areas of hyperactivity in the chemotherapy-treated twin relative to the untreated twin, which the authors interpreted as areas of deficits due to chemotherapy.

[Read "Lifting the Fog on Chemobrain" from CURE's summer 2011 issue]

Findings of several functional brain imaging studies have been reviewed by Reuter-Lorenz and Cimprich, and relative to “controls,” individuals treated with chemotherapy have been found to exhibit functional differences, including both areas of hyper- and hypoactivity during tasks, as well as differences in brain activity while the brain is at rest.

In addition, structural differences have been noted as well. Researchers compared brain images of women with breast cancer, some of whom received chemotherapy and some did not, and found decreases in volume and density of both white and grey matter in the group treated with chemotherapy. Chemotherapy-related reductions in grey matter have also been correlated with impairment in cognitive abilities.

Researchers have constructed a model detailing a proposed mechanism by which cancer treatment may lead to cognitive changes: Cancer treatment (chemotherapy but also including surgery, radiation treatment and hormonal therapy) combined with other clinical factors (inflammation, stress, fatigue, comorbidities and co-occurring symptoms) lead to cytokine dysregulation, hormonal changes and neurotransmitter dysfunction. This process, which may be moderated by baseline cognitive function, genetic variations, and age, combine to create cognitive changes. Researchers have put forth another model in which chemotherapy increases oxidative stress and inflammation, and decreases brain vascularization, neurogenesis and growth factors, and catecholamines.

These processes combine to decrease hippocampal function, leading to impaired learning and memory, and decrease frontal cortex function, which hinders planning and decision-making.

What Treatments Are Available?

The National Comprehensive Cancer Network’s Guidelines on Cognitive Function assert that despite increasing evidence of the validity of cancer-related cognitive dysfunction, there is limited evidence regarding treatment. Healthcare professionals are urged to validate patient concerns, provide education and to assess for contributing factors, including medications, depression, anxiety, pain, fatigue, substance abuse and sleep disturbance. Imaging studies are only recommended in specific situations.

Although most patients eventually return to pretreatment baseline, a subset report significant impairment in quality of life, independence and self-confidence. One of the most important things physicians can do is to provide emotional support by listening to the patient’s concerns and validating the existence of chemobrain.
It is common for families, coworkers and friends (and sometimes even healthcare professionals) to not understand that the emotional, physical or cognitive effects of cancer treatment may linger after treatment has ended. In a review of treatments for chemobrain, researchers categorized treatment into pharmacologic and non-pharmacologic interventions. The review documented that so far there is no strong evidence supporting the effectiveness of medications for chemobrain. Trials have explored the use of psychostimulants and drugs used to treat dementia; however, results have been mixed, and further research is needed.
Erythropoietinstimulating agents have also been tested, but due to concerns with adverse effects, they are not recommended for this purpose. Despite advertisements touting the effectiveness of their own programs, currently no strong evidence exists that computerized cognitive training produces significant, lasting, cognitive benefits.

Thankfully, non-pharmacologic strategies are available, including exercise, mindfulness, social support, and organizational strategies (See Box). Perhaps the largest body of evidence supports exercise to boost cognitive function, although much of the research in this area has been conducted with noncancer populations. Several studies with cancer patients have documented the effectiveness of exercise, including Qigong, Tai Chi, physical fitness, and resistance training to alleviate the symptoms of chemobrain.

One review documented that structured cognitive training programs, addressing memory, attention and processing speed have been promising, but the programs are not generally available outside of clinical trials. One final note: A recent study found that loneliness increases the risk of cognitive problems among breast cancer survivors. Encouraging increased socialization for those at risk of being lonely may be helpful.
Photo
CreditHanna Barczyk
A MONTH ago, I felt that I was in good health, even robust health. At 81, I still swim a mile a day. But my luck has run out — a few weeks ago I learned that I have multiple metastases in the liver. Nine years ago it was discovered that I had a rare tumor of the eye, an ocular melanoma. Although the radiation and lasering to remove the tumor ultimately left me blind in that eye, only in very rare cases do such tumors metastasize. I am among the unlucky 2 percent.
I feel grateful that I have been granted nine years of good health and productivity since the original diagnosis, but now I am face to face with dying. The cancer occupies a third of my liver, and though its advance may be slowed, this particular sort of cancer cannot be halted.
It is up to me now to choose how to live out the months that remain to me. I have to live in the richest, deepest, most productive way I can. In this I am encouraged by the words of one of my favorite philosophers, David Hume, who, upon learning that he was mortally ill at age 65, wrote a short autobiography in a single day in April of 1776. He titled it “My Own Life.”
“I now reckon upon a speedy dissolution,” he wrote. “I have suffered very little pain from my disorder; and what is more strange, have, notwithstanding the great decline of my person, never suffered a moment’s abatement of my spirits. I possess the same ardour as ever in study, and the same gaiety in company.”
I have been lucky enough to live past 80, and the 15 years allotted to me beyond Hume’s three score and five have been equally rich in work and love. In that time, I have published five books and completed an autobiography (rather longer than Hume’s few pages) to be published this spring; I have several other books nearly finished.
Hume continued, “I am ... a man of mild dispositions, of command of temper, of an open, social, and cheerful humour, capable of attachment, but little susceptible of enmity, and of great moderation in all my passions.”
Here I depart from Hume. While I have enjoyed loving relationships and friendships and have no real enmities, I cannot say (nor would anyone who knows me say) that I am a man of mild dispositions. On the contrary, I am a man of vehement disposition, with violent enthusiasms, and extreme immoderation in all my passions.
And yet, one line from Hume’s essay strikes me as especially true: “It is difficult,” he wrote, “to be more detached from life than I am at present.”
Over the last few days, I have been able to see my life as from a great altitude, as a sort of landscape, and with a deepening sense of the connection of all its parts. This does not mean I am finished with life.
On the contrary, I feel intensely alive, and I want and hope in the time that remains to deepen my friendships, to say farewell to those I love, to write more, to travel if I have the strength, to achieve new levels of understanding and insight.
This will involve audacity, clarity and plain speaking; trying to straighten my accounts with the world. But there will be time, too, for some fun (and even some silliness, as well).
I feel a sudden clear focus and perspective. There is no time for anything inessential. I must focus on myself, my work and my friends. I shall no longer look at “NewsHour” every night. I shall no longer pay any attention to politics or arguments about global warming.
This is not indifference but detachment — I still care deeply about the Middle East, about global warming, about growing inequality, but these are no longer my business; they belong to the future. I rejoice when I meet gifted young people — even the one who biopsied and diagnosed my metastases. I feel the future is in good hands.
I have been increasingly conscious, for the last 10 years or so, of deaths among my contemporaries. My generation is on the way out, and each death I have felt as an abruption, a tearing away of part of myself. There will be no one like us when we are gone, but then there is no one like anyone else, ever. When people die, they cannot be replaced. They leave holes that cannot be filled, for it is the fate — the genetic and neural fate — of every human being to be a unique individual, to find his own path, to live his own life, to die his own death.
I cannot pretend I am without fear. But my predominant feeling is one of gratitude. I have loved and been loved; I have been given much and I have given something in return; I have read and traveled and thought and written. I have had an intercourse with the world, the special intercourse of writers and readers.
Above all, I have been a sentient being, a thinking animal, on this beautiful planet, and that in itself has been an enormous privilege and adventure.

Friday, February 13, 2015

The Cancer That's Poised To Explode

Not long ago, a new medical epidemic arose: "the cancer." When people started to live longer, their aging bodies began to succumb to this disease we only poorly understood. Looking back, it is clear that much has changed for the better.
As we recognize World Cancer Day 2015, we have a lot to celebrate. By a number of measures, we are on our way to beating cancer. The Susan G. Komen foundation is arguably the most powerful medical advocacy organization the world has ever seen, and the growing awareness of lung cancer has nearly suffocated the multi-billion dollar tobacco industry. In almost all corners of the world, we are beginning to live and act in ways that lower our risk of getting cancer.
But the story is not only of progress. Though we've made leaps in our abilities to prevent, treat, and manage "the cancer," our success remains patchwork.
A quick pop quiz demonstrates the point. One-third of all cancer diagnoses are for cancer of the ________. a) bones; b) skin; c) pancreas; d) colon.
One doubts that many would have answered "skin" with any degree of confidence. And that's too bad, because many cases of skin cancer are preventable. But we're not paying attention.
In the past decade, we have seen a magnificent proliferation of the "heart healthy" icons on our foods. But where's the "skin healthy" icons on our soaps, lotions, and sunscreens? And as the NFL and Major League Baseball have brought the Komen Foundation's signature pink to cleats, gloves, bats, and penalty flags, where are the symbols for skin cancer?
Out of sight, out of mind.
Looking ahead, skin cancer is poised to explode. As people live longer -- as individuals routinely celebrate their 80th, 90th, and even 100th birthdays -- their skin will deteriorate. And with this deterioration comes an increase in susceptibility to cancer. This decline is, at the moment, nearly inevitable. That needs to stop. Healthy skin in older age is possible -- and it's an enabler of healthy aging.
This conclusion was reached at the first summit of its kind in Manchester, England, in June of 2014. A cross-sector group of experts from medicine, innovation, economics, and demography convened and agreed that a "life-course of healthy skin" is a pillar ofhealthy and active aging in the 21st century.
Moreover, it was also agreed that the need for healthy skin was pressing, given the rate at which the population is aging and the increased risk that older adults have in contracting skin cancer.
The data is powerful. Of all cases of non-melanoma skin cancer, more than 80 percent occur in people over 60. And over half of melanoma skin cancers occur in people over 50.
And, with nearly one-third of the U.S. population over 55 within the next five years, it is not only a health imperative to become more proactive in caring for our skin -- but also a social and economic imperative. In other "old" societies like Europe and Japan, the imperative is even greater. In emerging markets, which are still "younger" but are aging at breakneck pace, there is also no time to waste.
To elevate skin cancer to its rightful place at the top of our public health agenda, we will need to see strategies from both public and private leaders.
What Policymakers Can Do
In case you missed it, Congress and Obama signed the Sunscreen Innovation Act at the close of 2014. This was a smart move. It will streamline the FDA review and ingredient approval process so better, more innovative sunscreens can make it to supermarket shelves at a faster pace.
It's a step in the right direction, but let's use World Cancer Day to demand more action from the White House and Capitol Hill. Let's leverage World Cancer Day to get better sunscreens out of the shadows of the FDA's filing system.
Even more, let's ensure that this piece of legislation triggers a basic public policy shift where spending on health - including innovative medicines -- is seen as an investment in healthy aging that will have huge payback. From FDA regulations to government pricing policies, the next wave of innovative cancer medicines will be facilitated by a supportive environment innovation.
What Health Companies Can Do
If history is any guide, we are best at beating diseases when science, innovation, and business strategy come together. Looking at skin health as well as cancer treatment and prevention, we might be witnessing the first sign of such a marriage. Reuters recently reported that Nestle is planning to open 10 "skin care research centers" worldwide.
This is the latest sign that Nestle is investing seriously in dermatology, with a particular interest in age-related skin conditions. Nestle's Galderma, which has been in the skin health business for decades, is showing a commitment to a life course of healthy skin for all of us. This includes skin cancer, of course, but it also stretches to other conditions of our aging skin, which, when addressed, will lead to a healthier aging.
This World Cancer Day, let's reflect on our tremendous progress. Since "the cancer" was first recognized as a lethal disease, we've made remarkable strides in prevention and treatment. But it's time to broaden our lens. Our skin is our first line of defense, and also the site of one-third of all diagnosed cancers.
Michael Hodin Headshot

Friday, February 6, 2015

Glowing compound could lead to more effective cancer surgery

January 8, 2015
Scientists have developed a a new method that sees cancer cells glow, potentially allowing...
Scientists have developed a a new method that sees cancer cells glow, potentially allowing for more accurate surgeries (Image: Shutterstock)
Image Gallery (2 images)
Scientists from Oregon State University (OSU) have developed a new method that could make for better precision in the killing of cancer cells. The technique puts to use a unique compound with the ability to illuminate cancerous cells when exposed to near-infrared light, potentially acting as markers for surgeons taking on the intricate task of tumor removal.
The compound in question, known as naphthalocyanine, has three useful attributes once it has been exposed to near-infrared light. It can warm cancer cells and kill them off, it generates reactive oxygen species that can also cause the cancer cells to die, and it glows to serve as a potential marker for surgeons.
However, one weakness of naphthalocyanine is that it isn't water soluble, meaning that once it enters the body it tends to form clumps, foregoing its ability to make cells glow and produce the reactive oxygen species. On the plus side, the compound's properties can be manipulated by exposing it to different light intensities. So, by applying just the right amount of near-infrared light, it can be used to kill off only cancerous cells and leave healthy tissue unharmed.
To overcome its aversion to water, the researchers used a special water-soluble polymer called dendrimer. This enables the naphthalocyanine to travel inside a molecule that is attracted only to cancer cells and not healthy tissue. Once attached to the tumor, the scientists applied the required intensity of light, illuminating the cancer cells for the surgeons to more easily determine which tissues need removing. Completing the two-pronged attack, the lighting was optimized to activate the heating ability of the naphthalocyanine, killing off the cancer cells that might still linger following surgery.
The scientists performed their studies with laboratory mice, which showed no side effects. They say the technique shows great promise in improving the success rate of cancer treatments.
"With this approach, cancerous cells and tumors will literally glow and fluoresce when exposed to near-infrared light, giving the surgeon a precise guide about what to remove," says Oleh Taratula, an assistant professor in the OSU College of Pharmacy. “That same light will activate compounds in the cancer cells that will kill any malignant cells that remain. It’s an exciting new approach to help surgery succeed.”
Like-minded researchers have developed similar techniques in the past, involving different instruments and varying approaches. Early last year, scientists at Washington University produced a set of goggles through which surgeons could see cancer cells as a blue glow. Meanwhile, back in 2010 a device called the SpectroPen emerged, which was designed to make the edges of a tumor more visible during surgery.
But the OSU team says its approach could lead to a cheaper, more effective method than other solutions, and with less side effects. Next, it plans to perfect the process and test it on dogs with malignant tumors.
The research was published in the journal Nanoscale.