Differentiating Between Healthy Cells And Cancer Cells
Main Category: Cancer / OncologyAlso Included In: IT / Internet / E-mail; Stem Cell Research; Biology / Biochemistry
Article Date: 06 Jan 2009 - 7:00 PDT
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One of the current handicaps of cancer treatments is the difficulty of aiming these treatments at destroying malignant cells without killing healthy cells in the process. But a new study by McMaster University researchers has provided insight into how scientists might develop therapies and drugs that more carefully target cancer, while sparing normal healthy cells
Mick Bhatia, scientific director of the McMaster Stem Cell and Cancer Research Institute in the Michael G. DeGroote School of Medicine, and his team of investigators have demonstrated - for the first time - the difference between normal stem cells and cancer stem cells in humans.
The discovery, published in the prestigious journal Nature Biotechnology, could eventually help with the further customization and targeting of cancer treatments for the individual patient. It will immediately provide a model to discover drugs using robotic screening for available molecules that may have untapped potential to eradicate cancer.
"Normal stem cells and cancer stem cells are hard to tell apart, and many have misconstrued really good stem cells for cancer stem cells that have gone bad - we now can tell the ones masquerading as normal stem cells from the bad, cancerous ones," said Bhatia.
"This also allows us to compare normal versus cancer stem cells from humans in the laboratory - define the differences in terms of genes they express and drugs they respond to. Essentially, we can now use this to find the "magic bullet", a drug or set of drugs that kill cancer stem cells first, and spare the normal healthy ones," he said.
"McMaster is uniquely positioned for this discovery platform, and this was the missing ingredient - we have one of the best screening/robotic platforms, chemical libraries and expertise in professors Eric Brown and Gerry Wright, who have discovered molecules to combat infectious disease. Now we can combine it all. This team now aims to kill cancer."
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This work is funded by the Canadian Institutes of Health Research, the Canadian Cancer Society; the Ontario Institute for Cancer Research and the National Cancer Institute of Canada.
Source: Veronica McGuire
McMaster University
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Differentiating Between Normal Stem Cells And Cancer Stem Cells
posted by Gregory D. Pawelski on 6 Jan 2009 at 6:11 pmStem cells have that infinite ability to renew themselves and produce the many different cell types that make up a human. Cancer's hallmark is its ability to grow infinitely, multiplying into various cells that make up a tumor. Is cancer the result of a normal stem cell turned bad or an ordinary cell that somehow acquires a stem cell's immortality and versatility?
Being able to find out the difference between normal stem cells and cancer stem cells in humans will undoubtedly provide insight into developing therapies and drugs that more carefully target cancer, while sparing normal healthy stem cells. To prevent cancer's return may require one therapy to shrink a tumor and another therapy to kill the abnormal seeds that sprouted it. Newer treatments need to decrease the number of cancer stem cells.
Every tissue and organ in the body is made of cells. In order for cells to grow, divide, or die, they send and receive chemical messages. These messages are transmitted along specific pathways that involve various genes and proteins in a cell. There is a communication between stem cells and a tumor. It sends out a signal that make the different cells of the tumor and the cancer cells then (send chemical messages) that cycle back to the cancer stem cell.
A protein that governs development of human embryonic stem cells can inhibit the growth and spread (metastasis) of cancer. Embryonic stem cells can become any of 200-plus cell types in the adult body, depending on the signals they receive from their 'microenvironment' (surrounding cells, tissues and vasculature). During cancer progression, malignant cells also receive and release signals from their 'microenvironment,' cues that promote tumor growth and metastasis.
Finding the protein that prevents cancer from metastasizing, isolating factors within the human embryonic stem cell 'microenvironment,' can influence tumor cell fate and reverse the cancerous properties of metastatic tumor cells. However, it is not the only tumor suppressive factor within the embryonic 'microenvironment.' Not all genes and proteins have a critical role in the survival and growth of cancer cells.
In some cases, targeted drugs may kill tumor cells without killing microvascular cells in the same time frame. In other cases, they may kill microvascular cells without killing tumor cells. Yet in other cases, they could kill both types of cells or neither type of cells. The ability to these targeted agents to kill tumor and/or microvascular cells in the same tumor is highly variable among the different agents.
You still need to measure the net result of all cellular processes, including interactions, occurring in real time when cancer cells actually are exposed to specific cancer drugs, not just the individual molecular targets. Improving cancer patient diagnosis and treatment through a combination of cellular and gene-based testing will offer predictive insight into the nature of an individual's particular cancer and enable oncologists to prescribe treatment more in keeping with the heterogeneity of the disease.
Sources:
Cell Function Analysis
European Science Foundation
BMJ 2007; 334(suppl_1):s18 (6 January)
American Association for Cancer Research
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