Cancer cells are voracious eaters. Like a swarm of locusts, they devour every edible tidbit they can find. But unlike locusts, when the food is gone, cancer cells can’t just move on to the next horn o’ plenty. They have to survive until more food shows up — and they do.
Mei Kong, Ph.D., assistant professor in the Department of Cancer Biology, recently received $1.7 million from the National Cancer Institute to understand how cancerous cells survive their self-imposed famines.
Glutamine is an essential form of food for cancer cells. The amino acid provides the energy the cells need to survive and multiply. But malignant cells are gluttons and grow so rapidly they run through the glutamine stores, leaving themselves without their nutrition source. Although this should cause the cells to starve to death, it doesn’t.
Kong is working to uncover the tricks cancer cells use to stifle their hunger until the famine again turns to feast. So far she and her colleagues have found several proteins and molecular pathways involved in the process. The current grant will help them extend their studies, furthering our investment in scientific discovery to uncover possible new cancer therapies.
On Jan. 1, 2015, six City of Hope patients who have journeyed through cancer will welcome the new year with their loved ones atop City of Hope’s Tournament of Roses Parade float. The theme of the float is “Made Possible by HOPE.” The theme of the parade is “Inspiring Stories.”
Representing City of Hope’s nursing and clinical care teams will be Anne Bourque, R.N., clinical nursing director in the Department of Hematology & Hematopoietic Cell Transplantation. But Bourque also has her own patient story to tell. Here, the 35-year veteran of City of Hope relates her experience with colon cancer.
By Anne Bourque
I have two stories: one as an employee of City of Hope, and one as colon cancer survivor treated at City of Hope.
I am a registered nurse and started working at City of Hope in 1980 when I was 25. I can honestly say accepting a job here was one of the best decisions that I have made in my life. I have worked with some of the most talented and remarkable colleagues, and knowing many of them for 30-plus years has enriched my life tremendously.
Fast forward to 2002: Then, as now, I was the clinical nursing director of hematology and hematopoietic stem cell transplantation. I was divorced, with two children – Elizabeth, who was 19, and Gregory, who was 14.
I was 47, had some bleeding and went for a colonoscopy at a different hospital. I had no desire to have any City of Hope physician see me with less than my normal work clothes on, so naturally, I would have the test done elsewhere.
On Feb. 13, on the colonoscopy table, I found out that I had colon cancer. » Continue Reading
When 25-year-old Angelina Mattos was diagnosed with Stage 4 oral cancer earlier this year, she learned that her only hope of survival was through the removal of her tongue, a surgery that leaves people without the ability to talk or eat normally, sometimes permanently ending their ability to speak.
After hearing the prognosis, her family wanted to record Mattos so they could still listen to her voice when she could no longer talk. They suggested she record herself reading children’s books in case she ultimately decided to have children.
But Mattos wouldn’t let them. She refused to let her family, or herself, believe she would never again speak. She decided that she would beat the odds, that she would indeed regain her ability to talk. (Watch her recent interview with CBS.)
That decision was a defining moment in the Pomona woman’s long, and unexpected, battle with oral cancer.
Two years ago, Joselyn Miller and her family sat together as stem cells from her brother’s bone marrow were infused into her – a precious gift of life that the family is excited to have the chance to pass to another patient in need.
Today, the stem cell recipient is healthy. Her 23-year-old son Rex, who joined Be the Match’s bone marrow registry during the Bone Marrow Transplant Reunion in support of his mother, has had a rare opportunity: He was found to be an ideal match for a 65-year-old man abroad who needed a stem cell transplant.
Even as the overall rate of oral cancers in the United States steadily declines, the rate of tongue cancer is increasing — especially among white females ages 18 to 44.
An oral cancer diagnosis, although rare, is serious. Only half of the people diagnosed with oral cancer are still alive after five years, according to the federal Centers for Disease Control and Prevention. In large part, that’s because of the late diagnoses of this disease. Early signs of this cancer in young adults can be easily overlooked by primary physicians.
Although the reason for the rise among young adults is unclear, people can take steps to reduce their risk of serious disease, especially a late-stage diagnosis.
Ellie Maghami, M.D., chief of head and neck surgery at City of Hope, offers this advice: » Continue Reading
When it comes to research into the treatment of hematologic cancers, City of Hope scientists stand out. One study that they presented this week at the annual meeting of the American Society of Hematology suggests a new standard of care for HIV-associated lymphoma, another offers promise for the treatment of relapsing or treatment-resistant lymphoma, and still another points to more effective treatment for acute lymphoblastic leukemia.
Researchers from the Hematologic Malignancies and Stem Cell Transplantation Institute at City of Hope shared their findings at the annual ASH meeting, held Dec. 6 through 9, in San Francisco. More than 20,000 hematology professionals attended the annual conference, which highlights the hottest topics in the field.
Here are some of the highlights: » Continue Reading
Patients with HIV-associated lymphoma may soon have increased access to the current standard of care for some non-HIV infected patients – autologous stem cell transplants.
Impressive new data, presented Monday at the annual meeting of the American Society of Hematology (ASH) in San Francisco, indicate that HIV-associated lymphoma patients who meet standard eligibility criteria for transplants of their own stem cells respond well to the treatment, even in centers that do not have HIV-specific expertise. HIV infection has historically been viewed as reason to rule out autologous stem cell transplant – the standard of care for non-infected patients with relapsed or treatment-resistant lymphoma – due to their compromised immune system.
The new study could change that perception. It was led by Joseph Alvarnas, M.D., director of Medical Quality and Quality, Risk and Regulatory Management and a physician investigator at the Hematologic Malignancies and Stem Cell Transplantation Institute at City of Hope, and colleagues at Johns Hopkins Hospital. The study builds on previous research at City of Hope, including a crucial 2001 publication that was among the first internationally to show these transplants were possible for HIV patients. » Continue Reading
On Jan. 1, 2015, six City of Hope patients who have journeyed through cancer will welcome the new year with their loved ones atop City of Hope’s Tournament of Roses Parade float. The theme of the float is “Made Possible by HOPE.” The theme of the Rose Parade is “Inspiring Stories.”
By Evan Braggs
City of Hope is a place of just that, “a City of Hope.”
It was June of 2004, when I became a patient at City of Hope. At the age of 19, I was diagnosed with a rare blood disease called aplastic anemia. Not having had as much as a broken bone or a need for any type of surgery, I had to be cursed with a blood disorder, I thought.
What I labeled as a curse turned out to be the most humbling experience and lesson I’ve learned to this day. I was blessed to have the opportunity to meet a City filled with wonderful and extraordinary people who, in some cases, have influenced some of my adulthood decisions.
City of Hope has provided me with not just a second chance at life, but much more than that. After receiving a successful bone marrow transplant in June of 2005 from an unrelated donor, I had a different outlook on life. » Continue Reading
The holidays can create an overwhelming urge to give to people in need — especially to sick children and families spending the holidays in a hospital room.
That’s a good thing. Holiday donations of toys and gifts can bolster the spirits, and improve the lives, of people affected by illness, and hospitals nationwide rely on the generosity of the public to help provide holiday cheer.
“Sometimes even the smallest gestures can mean the world to someone going through a difficult time,” said Renee Ortiz, L.C.S.W., a pediatric social worker at City of Hope.
But before scouring the shelves at the local mall, give some thought to what pediatric patients and their families actually want and need. The No. 1 item on children’s and young adults’ wish lists? Gift cards.
“Gift cards allow patients and their families to shop in many ways,” Ortiz said. “They can go to the store and pick out what they need. And for patients who are stuck in the hospital during the holiday season, they can shop online. It allows them to shop and look forward for their items to be delivered to them.”
Other popular gifts include educational toys, arts and craft kits, and movies. Check out the City of Hope website for a full list of gift ideas for kids, teens and young adults.
But one more thing … If you’re finding it hard to resist that adorable stuffed animal, try a little harder. At City of Hope, stuffed animals and plush toys are strongly discouraged. A number of patients suffer from weakened immune systems, and these toys can easily trap dust and other substances that can potentially make the children even sicker.
If you want to make your donation in person, call City of Hope’s Department of Pediatrics at 626-256,4673, ext. 65430. The team will arrange for a time to meet you and accept the gifts on behalf of City of Hope patients. The deadline for holiday donations is Dec. 19. If you would like to make a monetary donation, please include a note clearly explaining the purpose of the gift, e.g., a donation to the Department of Pediatrics for pediatric patient gifts, activities, etc.