A controversial weed killer may inadvertently act as a fertilizer
for human cancer cells — and scientists are closer to understanding how.
Not exact matches
Specifically, when capsaicin frequently binds to receptors within the
human central nervous system's TRPV1 channel (the sensory receptor system
for pain and heat detection), these receptors deplete and this depletion results in a whole host of benefits
for the central nervous system at large, including terminating
cancer cells, increasing the metabolic rate and digestive efficiency, increasing circulatory blood flow, and combatting inflammation, and making you feel better about the world.
Introducing
human prostate
cancer cell lines into mice, Wu and his colleagues saw a particular enzyme called MAOA activate a cascade of signals that made it easier
for tumor
cells to invade and grow in bone.
Carlo Croce, a
cancer researcher at Ohio State University in Columbus, and his colleagues created a diagram of interacting miRNAs
for normal body
cells by connecting them according to which genes they target and the function of those genes, in a way similar to analyses of
human social networks.
To hunt
for drugs that target these
cells, Piyush Gupta, a molecular biologist at the Broad Institute at the Massachusetts Institute of Technology, and colleagues genetically engineered ordinary
human cells so that they acquired some of the properties of
cancer stem
cells, including being impervious to chemotherapy.
Human papillomavirus 16 accounts
for about half of all cervical
cancers, but researchers reporting September 7 in the journal
Cell have found that not all infections are equal.
Several studies have supported a role
for cancer stem
cells in the aggressive brain tumors called glioblastoma, but those studies involved inducing
human tumors to grow in mice, and as such their relevance to
cancer in
humans has been questioned.
Professor Ali Tavassoli, who led the study with colleague Dr. Ishna Mistry, explains: «In an effort to better understand the role of HIF - 1 in
cancer, and to demonstrate the potential
for inhibiting this protein in
cancer therapy, we engineered a
human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed in a hypoxic environment.
Serendipitously, the antimicrobial peptide shows promise
for protecting
humans from
cancer; it can inhibit the growth of prostate and bladder
cancer cells, as well as multi-drug resistant leukemic
cells.
The researchers tested their technique by applying the light
for 1 minute to
human cervical
cancer cells surrounded with common anti-
cancer drugs such as epigallocatechin gallate (EGCG).
When the scientists inserted
human colorectal
cancer cells into zebrafish embryos and allowed them to grow
for 4 days, the resulting tumors showed three hallmarks of
human solid tumors: rapid
cell division, formation of blood vessels to supply nutrients, and the ability to spread to other locations in the body.
The second challenge to researching viral therapies
for childhood
cancers is the fact that mouse
cells don't get infected with
human viruses as easily as
human cells.
Then the researchers turned to the lab, where they exposed
human liver, breast, colon, ovarian, and other
cancer cells to the drugs, which appeared to make it easier
for the
cells to migrate.
In contrast, viruses that cause
cancer, such as the
human papillomavirus that is responsible
for most cases of cervical
cancer, disrupt a
cell's genome, thereby triggering out - of - control growth.
We employ similar pathways to shape our parts as embryos, but over the course of evolution,
humans may have lost the ability to tap into it as adults, perhaps because the
cell division required
for regeneration elevated the likelihood of
cancer.
«There are still many questions left to answer but we now know that oxygen poor environments, like those often found in advanced
human breast
cancers serve as nurseries
for the birth of
cancer stem cells,» says Gregg Semenza, M.D., Ph.D., the C. Michael Armstrong Professor of Medicine and a member of the Johns Hopkins Kimmel Cancer C
cancer stem
cells,» says Gregg Semenza, M.D., Ph.D., the C. Michael Armstrong Professor of Medicine and a member of the Johns Hopkins Kimmel
Cancer C
Cancer Center.
Exploiting the same pre-clinical model used
for their studies, the researchers are testing the efficacy of this kind of drug candidates against
cancer stem
cells, and the possibility of identifying combination regimens with standard chemotherapies with minimized toxic effects, with the perspective of their possible application
for the treatment of
human breast
cancer.
They tested these drugs one at a time
for lethal interaction with 112 different tumor - suppressor gene mutations in
human cancer cells growing in the lab.
«Researchers ID
cancer gene - drug combinations ripe
for precision medicine: Yeast,
human cells and bioinformatics help develop one - two punch approach to personalized
cancer therapy.»
Abnormal centrosome numbers are commonly observed in
human cancers and are thought to be at least in part responsible
for the improper distribution of the genetic material that is a hallmark of many
cancer cells.
His postdoc characterizing
human embryonic stem
cells resulted in seven papers and a contract position at the Center
for Cancer Systems Biology at Tufts University School of Medicine in 2009.
One postdoc presents data on her efforts to develop an organoid model
for small -
cell lung
cancer; another reports progress on culturing hormone - secreting organoids from
human gut tissue.
She helped lead a GSK project focused on designing a monoclonal antibody to link to the HER3 receptor on
human cells as a treatment
for cancer.
Now, scientists have modified Salmonella bacteria to trigger a particularly powerful immune response against
human cancer cells implanted in mice, shrinking the tumors and —
for the first time — preventing them from metastasizing.
The use of bone marrow - derived stem
cells is well established in the treatment of
human cancer patients, and veterinary applications
for bone marrow - and adipose - derived stem
cells are being evaluated.
Researchers at Rice University's Laboratory
for Systems Biology of
Human Diseases analyzed the metabolic profiles of hundreds of ovarian tumors and discovered a new test to determine whether ovarian
cancer cells have the potential to metastasize.
To test their hypothesis, the researchers carried out experiments on
human melanoma
cells, a line of
cancer cells they chose
for their ability to grow easily and quickly.
Human tumor tissue or cell lines can be coengrafted into these mouse models, providing a powerful tool for studying the interactions between human immune cells and human can
Human tumor tissue or
cell lines can be coengrafted into these mouse models, providing a powerful tool
for studying the interactions between
human immune cells and human can
human immune
cells and
human can
human cancers.
Her research is both translational and clinical in nature and centers on the
human genetics of healthy skin aging and diseases related to aging skin, including new treatments
for advanced basal
cell skin
cancers.
«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.
But while researchers have previously been able to infect cultures of
human hepatocytes with HBV, the
cells» limited lifespan has made it difficult to study the virus, says Bhatia, who is also a Howard Hughes Medical Institute investigator and a member of MIT's Koch Institute
for Integrative
Cancer Research and Institute
for Medical Engineering and Science.
«The LSC17 score is the most powerful predictive and prognostic biomarker currently available
for AML, and is the first stem
cell - based biomarker developed in this way
for any
human cancer,» says Dr. Wang.
«If further studies validate that these processes are critical in
human breast
cancers,» Koshy notes, «the possibility exists that agents that favorably modify the biophysical properties of the extracellular matrix, or that target the receptors and signaling molecules associated with how
cells sense this matrix, could be used as a new avenue
for the prevention or treatment of breast
cancers.»
It's not all just fun and games: Understanding how
cells — especially white blood
cells — navigate through the
human body could help scientists create better treatments
for cancer, infectious disease, and autoimmune disorders.
«
For example, mouse mammary tumors shared a signaling pathway that is found in
human lung
cancer and controls how
cells reproduce and move from one location to another.»
The results of this original study are highly relevant to other
human diseases that dependent on genome instability, such as fungal infection or
cancer, and open new venues
for anti-leishmanial drug discovery using host - directed strategies that target the parasite's metabolic dependence on the host
cell, thus preventing the adaptive evolution of drug resistant parasites.
If dealing with the public relations nightmare over its on - off - on funding of Planned Parenthood wasn't enough, the Susan G. Komen
for the Cure
cancer charity last week also got entangled, somewhat bizarrely, in the debate over
human embryonic stem (ES)
cell research.
The research, «Synchrotron X-Ray Fluorescence Nanoprobe Reveals Target Sites
for Organo - Osmium Complex in
Human Ovarian
Cancer Cells», is published in Chemistry — A European Journal.
Previous evidence
for a breast
cancer link has been mixed — one study found increased risk in women exposed before age 14, whereas others found no association — but in a lab dish, DDT has been shown to activate the HER2 gene in
human breast
cells, which is expressed in some breast
cancers.
The study, which is published in the journal Nature Communications, was conducted on
human tumour
cells and on mice, and offers hope of a much improved therapy
for a severe form of
cancer.
For this reason, the National Cancer Institute maintains a library of 60 authenticated human cancer cell lines for the purposes of research, called the NCI -
For this reason, the National
Cancer Institute maintains a library of 60 authenticated human cancer cell lines for the purposes of research, called the NCI
Cancer Institute maintains a library of 60 authenticated
human cancer cell lines for the purposes of research, called the NCI
cancer cell lines
for the purposes of research, called the NCI -
for the purposes of research, called the NCI - 60.
In a companion study also published in Science, Nick Haining, MD, and colleagues from Dana - Farber
Cancer Institute, also found a distinct epigenetic landscape
for exhausted T
cells in mice and
humans, and they were able to ascribe key functions in T
cell exhaustion to some of these epigenetic changes.
As part of the international EU project «SPICE II Plus,» which is now coming to an end, scientists from the MedUni Vienna's Institute
for Cancer Research have now also found evidence that synthetic substances damage the DNA of human cells and can therefore possibly have cancer - causing ef
Cancer Research have now also found evidence that synthetic substances damage the DNA of
human cells and can therefore possibly have
cancer - causing ef
cancer - causing effects.
But a computer game that puts those kids on the front line of a battlefield inside the
human body — where
cancer cells and chemotherapy drugs are slogging it out
for supremacy — just might persuade them that it's important to keep taking the drugs.
«In CRISPR advance, scientists successfully edit
human T
cells: Research has implications
for autoimmune diseases, AIDS,
cancer.»
The ability of the ITAM sequence to make
cells cancerous represents a potential new trigger
for breast
cancer in
humans, say the researchers, and gives further credence to the idea that viruses can cause
human breast
cancer.
For more than 25 years, scientists examining cultures of
human cancer cells have occasionally spotted
cells tucked within other
cells.
The
human genome contains around 20,000 genes, by refining CRISPR - Cas9 technology and using it to screen the leukemia genome the team uncovered a catalogue of approximately 500 genes that are essential
for cancer cell survival, including more than 200 genes
for which drugs could be designed.
For years researchers have been developing molecular imaging techniques that visualize hormonally active breast cancer cells — specifically those testing positive for human epidermal growth factor receptor 2 (HER
For years researchers have been developing molecular imaging techniques that visualize hormonally active breast
cancer cells — specifically those testing positive
for human epidermal growth factor receptor 2 (HER
for human epidermal growth factor receptor 2 (HER2).
The study has important implications
for human health, and is particularly useful
for understanding the changes that occur in
cells during the development of the tumors that underlie
cancers.