A number of laboratory
studies on cancer cells have shown that curcumin does have anticancer effects.
Some of them come from
studies on cancer cells, which can blunt the immune system.
Not exact matches
Baylin and Johns Hopkins scientist Michelle Vaz, Ph.D., first author
on the
study, suspected that the interplay of epigenetic and genetic changes may occur when normal lung
cells develop into
cancer, but, Baylin says, the timing of such changes was unknown.
The
study, led by Dr Len Stephens and Dr Phill Hawkins and published today in the journal Molecular
Cell, reveals why loss of the PTEN gene has such an impact
on many people with prostate
cancer, as well as in some breast
cancers.
Based
on results of the current
study described in a report online June 18 in the journal
Cancer Cell, Johns Hopkins researchers say they are planning a phase I clinical trial to test the paclitaxel - fostamatinib combination therapy in patients with recurrent advanced ovarian c
Cancer Cell, Johns Hopkins researchers say they are planning a phase I clinical trial to test the paclitaxel - fostamatinib combination therapy in patients with recurrent advanced ovarian
cancercancer.
Fostamatinib's effect
on microtubules seems to increase the stabilizing effect of paclitaxel, even in resistant
cells, which in turn may prevent
cancer cells from proliferating, says Yu Yu, Ph.D., a postdoctoral fellow at the Johns Hopkins University School of Medicine and co-author of the
study.
The idea to specifically
study this group of patients was based
on groundbreaking research Garon published in the New England Journal of Medicine last year, which found that among patients who received pembrolizumab, those with PD - L1 expression
on at least 50 percent of their
cancer cells showed the longest survival and disease control.
The protein puts the immune system's brakes
on, keeping its T
cells from recognizing and attacking
cancer cells, said Dr. Antoni Ribas, the
study's principal investigator and a professor of medicine in the division of hematology - oncology at the David Geffen School of Medicine at UCLA.
The
study, published April 4 in the journal The Lancet Oncology, focused
on non-small
cell lung
cancer, which is the most common form of lung
cancer.
In this
study, the SIgN team discovered for the first time that the integrity of p53 affects the production of a special
cell surface protein called Major Histocompatibility Complex (MHC) class I. MHC class I molecules
on the
cancer cell surface serve as targets for the immune system.
A
study analyzing brain tumor genomics
on a single -
cell level has found evidence that
cancer stem
cells fuel the growth of oligodendrogliomas, a slow - growing but incurable form of brain
cancer.
Bloch's colleagues at the National Institute of Environmental Health Sciences tested the oils in gene expression
studies on lab - grown human breast
cancer cells and found that they could mimic estrogens, the primary female sex hormones, and inhibit androgens, the primary male sex hormones.
Dr. Weiss»
study of pembrolizumab was presented during a session
on small
cell lung
cancer when the theme of the conference was Science Drives Lung Cancer Adv
cancer when the theme of the conference was Science Drives Lung
Cancer Adv
Cancer Advances.
This
study, published in the journal Microarrays, shows that lack of SOST in the bone microenvironment promotes the expression of many genes associated with
cell migration and / or invasion, including long non-coding RNA MALAT1 in prostate
cancer, suggesting that SOST has an inhibitory effect
on prostate
cancer invasion.
«Currently a majority of patients undergo colon resections for large polyps that don't harbor any
cancer cells, which means in many cases a person's colon is being removed for noncancerous reasons, based
on subjective criteria,» said lead
study author Emre Gorgun, MD, FACS, FASCRS, a staff surgeon in the department of colorectal surgery, Cleveland Clinic, Ohio.
ON THE ROAD Breast
cancer cells may break away from the main tumor in clumps, already bearing most of the mutations that will drive
cancer recurrence, a
study suggests.
Previous
studies of genetic alterations in lymphoma and lung
cancer have found that certain genetic mutations — specifically when part of a gene breaks off and gets fused to another — can inappropriately switch
on ALK, driving
cancer cells to grow and divide.
«Because 85 percent of people in the
study reported extending the antenna during calls, we might have expected to find a disproportionate cluster of tumors behind the eye and the ear
on the side the
cell phone was used since radiation emission is highest at the antenna,» says co-author Mark Malkin, a neuro - oncologist at Memorial Sloan - Kettering
Cancer Center.
In this
study, we found that chloroquine not only has an effect
on the growth of the
cancer cells, but also makes the tumor environment less aggressive by normalizing the abnormal blood vessels in the tumor,» says Patrizia Agostinis.
For this
study, Nakano and his collaborators used
cancer cells from 40 patients with high - grade gliomas, focusing
on tumor
cells with a stem -
cell signature.
In a related
study, published online
on March 27 in the same journal, Green's group also showed that a different particle formulation could effectively carry and deliver so - called siRNAs to brain
cancer cells.
With a view to clinical
studies (tests
on humans) it is important to note that the effects
on the tumor vasculature were even observed at chloroquine concentrations that had little effect
on autophagy in the
cancer cells.
The
study builds
on previous findings suggesting that AIM2 limits
cancer cell growth in colon
cancer cell lines, Wilson said, as well as
on a clinical report of poor prognosis in colon
cancer patients with low or missing AIM2 levels.
To see whether
cancer stem
cell renewal involves a chain of events similar to that used by embryonic stem
cells, and whether the process was affected by oxygen levels, Semenza and graduate student Chuanzhao Zhang focused their
studies on two human breast
cancer cell lines that responded to low oxygen by ramping up production of the protein ALKBH5, which removes methyl groups from mRNAs.
In the context of the current
study, the researchers have developed a pre-clinical model system that specifically captures the impact of a treatment
on cancer stem
cells.
Professor Gianni Liti, a senior author
on the paper from the Institute for Research
on Cancer and Ageing, Nice, said: «We were able to
study the evolution in time by combining genome sequences of the
cell populations and tracking the growth characteristics of the yeast
cells.
Based
on the pioneering work of Dr. Claire Lugassy and Dr. Raymond Barnhill at UCLA's Jonsson Comprehensive
Cancer Center, a new study provides additional support for a process by which melanoma cells, a deadly form of skin cancer, can spread throughout the body by creeping like tiny spiders along the outside of blood vessels without ever entering the blood stream, and that this process is exacerbated by exposure to ultraviolet (UV)
Cancer Center, a new
study provides additional support for a process by which melanoma
cells, a deadly form of skin
cancer, can spread throughout the body by creeping like tiny spiders along the outside of blood vessels without ever entering the blood stream, and that this process is exacerbated by exposure to ultraviolet (UV)
cancer, can spread throughout the body by creeping like tiny spiders along the outside of blood vessels without ever entering the blood stream, and that this process is exacerbated by exposure to ultraviolet (UV) light.
The
study found that combining the two drugs had an increased effect of killing of
cancer cells, while individually, the drugs have considerably less impact
on cell viability.
After a median follow - up of 11 months, 11 of the 13 patients who responded remain
on the
study, including one patient who had non-small
cell lung
cancer (NSCLC) with a ROS1 gene fusion who has had a complete response that has been maintained for more than two years.
Ana Soto, professor of cellular biology at Tufts University School of Medicine, and her colleagues were
studying the effects of estrogen
on a breast
cancer cell line.
Lead author Moustafa Abdalla writes: «Almost all genomic
studies of breast
cancer have focused
on well - established tumours because it is technically challenging to
study the earliest mutational events occurring in human breast epithelial
cells.»
After completing her graduate
studies in 2006, she joined the laboratory of Dr. Craig B. Thompson at the University of Pennsylvania for postdoctoral work focusing
on cancer cell metabolism.
The researchers have isolated the sesquiterpene lactone damsin from the plant and
studied its effect
on cancer stem
cells in three different breast
cancer cell lines.
With this context, the new
study tested an approach based
on the idea that if prostate
cancer cells were flooded with testosterone, the
cells might be killed by the hormone shock.
Co-senior
study investigator and
cancer biologist Iannis Aifantis, PhD, says the
study offers the first evidence that «drugs targeting and disrupting leukemia
cells» microenvironment — or what goes
on around them — could prove effective against the disease.»
The
study builds
on Polyak's earlier research finding that women already identified as having a high risk of developing
cancer — namely those with a mutation called BRCA1 or BRCA2 — or women who did not give birth before their 30s had a higher number of mammary gland progenitor
cells.
A new
study led by scientists from the Florida campus of The Scripps Research Institute (TSRI) sheds light
on a signaling circuit in
cells that drives therapy resistance in prostate
cancer.
In fact, depending
on the tumor
cell, they grow at dramatically different speeds, according to a
study led by Nicholas Navin, Ph.D., assistant professor in the Department of Genetics at The University of Texas M.D. Anderson
Cancer Center in Houston.
Prof Hans Clevers, from Hubrecht Institute in the Netherlands, joint corresponding author
on the paper, said: «Organoids had not been used to
study single
cancer cells before.
She set up a lab dedicated to
studying the effects of chemokines
on cell death and
cancer.
Co-authors
on the
study were Christian Mosimann (University of Zürich), Zi Peng Fan (Whitehead Institute and MIT), Justin Tan (Genome Institute of Singapore), Richard White (Memorial Sloan Kettering
Cancer Center), Dominick Matos (Massachusetts General Hospital), Ann - Christin Puller (University Medical Center Hamburg - Eppendorf, Germany), Eric Liao (Harvard Stem
Cell Institute and MGH) Richard Young (Whitehead Institute and MIT), and, at Boston Children's Hospital, Song Yang, Andrew Thomas, Julien Ablain, Rachel Fogley, Ellen van Rooijen, Elliott Hagedorn, Christie Ciarlo and Cristina Santoriello.
In this
study, the researchers tested the effects of Olaparib
on the tumors formed by human breast
cancer cells injected into mice.
Currently, in another
study, the researchers are focused
on detecting circulating tumor
cells in the blood of patients with a diagnosis of breast
cancer.
«This
study also provides new information
on a method to reduce or eliminate
cancer cell exposure during the fertility preservation process,» she adds.
«With further research we hope to create a nontoxic nanocarrier that could provide targeted delivery of the TM - 025 and TM - 026 analogs specifically to
cancer cells,» said Gitali Indra, an OSU assistant professor and also a lead and corresponding author
on the
study.
«A traditional view of chemotherapy is that you try to completely kill
cancer cells and destroy tumors,» said Arup Indra, an associate professor in the OSU College of Pharmacy and one of the lead authors
on the
study.
«We challenged a current dogma in the field that emphasized PLK1's role in mitosis (
cell division) as a primary mechanism for
cancer growth,» says Zheng Fu, Ph.D., lead investigator on the study, member of the Cancer Molecular Genetics research program at VCU Massey Cancer Center and assistant professor in the Department of Human and Molecular Genetics at the VCU School of Med
cancer growth,» says Zheng Fu, Ph.D., lead investigator
on the
study, member of the
Cancer Molecular Genetics research program at VCU Massey Cancer Center and assistant professor in the Department of Human and Molecular Genetics at the VCU School of Med
Cancer Molecular Genetics research program at VCU Massey
Cancer Center and assistant professor in the Department of Human and Molecular Genetics at the VCU School of Med
Cancer Center and assistant professor in the Department of Human and Molecular Genetics at the VCU School of Medicine.
In a four - year
study conducted
on the mouse model in advanced breast
cancer metastasis in the eye's anterior chamber, Petty and colleagues found that the new nanoparticle not only killed tumor
cells in the eye, but also extended the survival of experimental mice bearing 4T1 tumors, a
cell line that is extremely difficult to kill.
In the new
study, the researchers cultured mouse skin -
cancer colonies
on various 2 - D and 3 - D environments of different shapes and patterns to see if the tumor shape contributes to activation of
cancer stem
cells, and to see where in the tumor the stem
cells appeared.
In the new
study, Burrows and colleagues focused
on the protein HIC1, or «Hypermethylated in
cancer 1, «so named because it was first identified in
cancer cells; however, it also helps regulate gene expression in normal
cells.