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Stem Cells cause cancer?


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#1 Lazarus Long

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Posted 23 December 2007 - 02:58 PM


Here is an interesting argument that deserve more attention. It also describes a new way of looking at how to treat cancer that is emerging from a combined understanding of stem cells and epigenetics. Yet the hypothesis is somewhat old, but it keeps emerging like its metaphor and it returns again and again after opponents think it is irradiated when new evidence arrives to support it.

Stem Cell Theory of cancer

Scientists Weigh Stem Cells’ Role as Cancer Cause
Fabrizio Costantini for The New York Times

Posted Image
Dr. Max S. Wicha, a leading researcher of cancerous stem cells.

By GINA KOLATA
Published: December 21, 2007

Within the next few months, researchers at three medical centers expect to start the first test in patients of one of the most promising — and contentious — ideas about the cause and treatment of cancer. The idea is to take aim at what some scientists say are cancerous stem cells — aberrant cells that maintain and propagate malignant tumors.

Although many scientists have assumed that cancer cells are immortal — that they divide and grow indefinitely — most can only divide a certain number of times before dying. The stem-cell hypothesis says that cancers themselves may not die because they are fed by cancerous stem cells, a small and particularly dangerous kind of cell that can renew by dividing even as it spews out more cells that form the bulk of a tumor. Worse, stem cells may be impervious to most standard cancer therapies.

Not everyone accepts the hypothesis of cancerous stem cells. Skeptics say proponents are so in love with the idea that they dismiss or ignore evidence against it. Dr. Scott E. Kern, for instance, a leading pancreatic cancer researcher at Johns Hopkins University, said the hypothesis was more akin to religion than to science.

At stake in the debate is the direction of cancer research. If proponents of the stem-cell hypothesis are correct, it will usher in an era of hope for curing once-incurable cancers. If the critics are right, the stem-cell enthusiasts are heading down a blind alley that will serve as just another cautionary tale in the history of medical research. In the meantime, though, proponents are looking for ways to kill the stem cells, and say that certain new drugs may be the solution.

“Within the next year, we will see medical centers targeting stem cells in almost every cancer,” said Dr. Max S. Wicha, director of the University of Michigan Comprehensive Cancer Center, one of the sites for the preliminary study that begins in the next few months (the other participating institutions are Baylor College of Medicine in Houston and the Dana-Farber Cancer Institute in Boston).

“We are so excited about this,” Dr. Wicha said. “It has become a major thrust of our cancer center.”

At the National Cancer Institute, administrators seem excited, too.

“If this is real, it could have almost immediate impact,” said Dr. R. Allan Mufson, chief of the institute’s Cancer Immunology and Hematology Branch.

The cancer institute is financing the research, he said, and has authorized Dr. Mufson to put out a request for proposals, soliciting investigators to apply for cancer institute money to study cancer stem cells and ways to bring the research to cancer patients. The institute has agreed to contribute $5.4 million. “Given the current fiscal situation, which is terrible, it’s a surprising amount,” Dr. Mufson said. “We actually asked for less,” he added, but the cancer institute’s executive committee asked that the amount be increased.

Proponents of the hypothesis like to use the analogy of a lawn dotted with dandelions: Mowing the lawn makes it look like the weeds are gone, but the roots are intact and the dandelions come back. So it is with cancer, they say. Chemotherapy and radiation often destroy most of a tumor, but if they do not kill the stem cells, which are the cancer’s roots, it can grow back.

Cancerous stem cells are not the same as embryonic stem cells, the cells present early in development that can turn into any cell of the body. Cancerous stem cells are different. They can turn into tumor cells, and they are characterized by distinctive molecular markers.

The stem-cell hypothesis answered a longstanding question: does each cell in a tumor have the same ability to keep a cancer going? By one test the answer was no. When researchers transplanted tumor cells into a mouse that had no immune system, they found that not all of the cells could form tumors.

To take the work to the next step, researchers needed a good way to isolate the cancer-forming cells. Until recently, “the whole thing languished,” said Dr. John E. Dick, director of the stem cell biology program at the University of Toronto, because scientists did not have the molecular tools to investigate.

But when those tools emerged in the early 1990s, Dr. Dick found stem cells in acute myelogenous leukemia, a blood cancer. He reported that such cells made up just 1 percent of the leukemia cells and that those were the only ones that could form tumors in mice. Yet Dr. Dick’s research, Dr. Wicha said, “was pretty much ignored.” Cancer researchers, he said, were not persuaded — and even if they had accepted the research — doubted that the results would hold for solid tumors, like those of the breast, colon, prostate or brain. That changed in 1994, when Dr. Wicha and a colleague, Dr. Michael Clarke, who is now at Stanford, reported finding cancerous stem cells in breast cancer patients.

“The paper hit me like a bombshell,” said Robert Weinberg, a professor of biology at M.I.T. and a leader in cancer research. “To my mind, that is conceptually the most important paper in cancer over the past decade.”

Dr. Weinberg and others began pursuing the stem-cell hypothesis, and researchers now say they have found cancerous stem cells in cancers of the colon, head and neck, lung, prostate, brain, and pancreas. Symposiums were held. Leading journals published paper after paper. But difficult questions persisted. One problem, critics say, is that the math does not add up. The hypothesis only makes sense if a tiny fraction of cells in a tumor are stem cells, said Dr. Bert Vogelstein, a colon cancer researcher at Johns Hopkins who said he had not made up his mind on the validity of the hypothesis.

But some studies suggest that stem cells make up 10 percent or even 40 percent or 50 percent of tumor cells, at least by the molecular-marker criterion. If a treatment shrinks a tumor by 99 percent, as is often the case, and 10 percent of the tumor was stem cells, then the stem cells too must have been susceptible, Dr. Vogelstein says.

Critics also question the research on mice. The same cells that can give rise to a tumor if transplanted into one part of a mouse may not form a tumor elsewhere.

“A lot of things affect transplants,” Dr. Kern, the Johns Hopkins researcher, said, explaining that transplanting tumors into mice did not necessarily reveal whether there were stem cells.

Other doubts have been raised by Dr. Kornelia Polyak, a researcher at the Dana-Farber Cancer Institute. Dr. Polyak asked whether breast cancer cells remain true to type, that is, whether stem cells remain stem cells and whether others remain non-stem cells? The answer, she has found, is “not necessarily.”

Cancer cells instead appear to be moving targets, changing from stem cells to non-stem cells and back again. The discovery was unexpected because it had been thought that cell development went one way — from stem cell to tumor cell — and there was no going back.

“You want to kill all the cells in a tumor,” Dr. Polyak said. “Everyone assumes that currently-used drugs are not targeting stem cell populations, but that has not been proven.”

“To say you just have to kill the cancer stem cell is oversimplified,” she added. “It’s giving false hope.”

The criticisms make sense, Dr. Weinberg said. But he said he remained swayed by the stem cell hypothesis.

“There are a lot of unanswered questions, mind you,” he said. “Most believe cancer stem cells exist, but that doesn’t mean they exist. We believe it on the basis of rather fragmentary evidence, which I happen to believe in the aggregate is rather convincing.”

Dr. Wicha said he was convinced that the hypothesis was correct, and said it explained better than any other hypothesis what doctors and patients already know. “Not only are some of the approaches we are using not getting us anywhere, but even the way we approve drugs is a bad model,” he said. Anti-cancer drugs, he noted, are approved if they shrink tumors even if they do not prolong life. It is the medical equivalent, he said, of mowing a dandelion field.

He said the moment of truth would come soon, with studies like the one planned for women with breast cancer. The drug to be tested was developed by Merck to treat Alzheimer’s disease. It did not work on Alzheimer’s but it kills breast cancer stem cells in laboratory studies, Dr. Wicha says.

The study will start with a safety test on 30 women who have advanced breast cancer. Hopes are that it will be expanded to find out if the drug can prolong lives.

“Patient survival,” Dr. Wicha said, “is the ultimate endpoint.”


#2 Athanasios

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Posted 10 January 2008 - 10:41 PM

I was reading an article by R.J. Jones, of John Hopkins, where he talked of developing new measures of a successful drug

Because of the difficulty in assessing the effects of therapies on the
rare cancer stem cells responsible for relapse, the development of such
approaches requires new clinical paradigms and methodologies (Huff
et al. 2006). We believe these new paradigms should rely heavily on
preclinical modeling, employ nontraditional measures of clinical re-
sponse as trial end points, and utilize novel preclinical assays to eval-
uate the fate of cancer stem cells. Preclinical studies should assess the
effects of therapies on both cancer stem cell and differentiated cancer
cell populations.


He also talked of ways to eliminate the cancer stem cells despite their slow growth and immunites. One proposal is to use telomerase inhibitors. The idea being that cancer stem cells have shorter telomeres than normal ones so cancer stem cells will be more sensitive to the removal of telomerase and the existence of more primitive normal stem cells can replenish the pool if needed.

Anyway, thought I would pass it along.

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#3 s123

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Posted 10 January 2008 - 11:18 PM

Interesting article.

I was reading an article by R.J. Jones, of John Hopkins, where he talked of developing new measures of a successful drug

Because of the difficulty in assessing the effects of therapies on the
rare cancer stem cells responsible for relapse, the development of such
approaches requires new clinical paradigms and methodologies (Huff
et al. 2006). We believe these new paradigms should rely heavily on
preclinical modeling, employ nontraditional measures of clinical re-
sponse as trial end points, and utilize novel preclinical assays to eval-
uate the fate of cancer stem cells. Preclinical studies should assess the
effects of therapies on both cancer stem cell and differentiated cancer
cell populations.


He also talked of ways to eliminate the cancer stem cells despite their slow growth and immunites. One proposal is to use telomerase inhibitors. The idea being that cancer stem cells have shorter telomeres than normal ones so cancer stem cells will be more sensitive to the removal of telomerase and the existence of more primitive normal stem cells can replenish the pool if needed.

Anyway, thought I would pass it along.


Good idea but cancer cells can mutate and become resistant for the telomerase inhibitor. It's good as a temporally method to fight cancer but eventually the use of any drug will fail to cure every cancer. Dr. de Grey suggests another approach. He would kill all the stem cells in your body and then replace them by stem cells in which he has deleted the gene for telomerase and ALT. He calls this concept the whole body interdiction of the lengthening of telomeres (WILT).

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#4 Hedgehog

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Posted 13 February 2008 - 11:57 PM

There is a current theory that Adult Stem Cells (ASC) cause cancer (like the articles you listed above). From the reading I have done it seems like pathways that are turned on during repairing events sometimes get stuck on.

Embryonic Stem Cells


The Embryonic pathways helps to cause cell proliferation and morphogenesis of Embryonic Stem Cells (ESC). Stems cells have unique properties. These properties include self-renewal and they can become specialized cells such as nerves, muscles, bone...ect. pathway target genes cause cell division and with different degrees of pathway activities can produce stem cells to become specialized cells.

ASC

In the adult, the embryonic pathways are normally quiescent. However, some of these pathways have been shown to be active in a few cells that are normally dividing at a high rate. Your body has adult stem cells that are used for repairing or renewal of old or damaged cells. For example if you get hurt or damage your cells have to be repaired! When tissue is damage the a few pathways are turned on and causes adult cells to divide and turn into the correct linage. The Hh (hedgehog) is most likely not the only pathway that can do this but appears to be a master regulator that turns on other pathways that are essential for the repair and regeneration process. This is similar to how the Hh operates on embryonic stem cells, but because the adult body is not growing and is fully developed it does not need the hedgehog pathway turned on all the time.

Cancer and ASC

Cancer is caused by a genetic mutation that occurs by a carcinogen. Carcinogens are often chemicals such as cigarette smoke or other environmental factors. Carcinogens cause the genetic code of a cell(s) to change. This change leads to a genetic lesion and sometimes allows a cell to be unregulated and proliferate. A very simplified view is an adult stem cell gets stuck in continual repair which leads to cancer. Cells that are repeatedly subjected to carcinogens often have a higher chance of turning cancerous. For example, skin cancer (uv radiation) & lung cancer (smokers). While the Hedgehog pathway appears to play a key role in post embryonic patterning, it is not a magic bullet for cancer. Hh antagonist are specific thus they may lead less side effects compared to current cytotoxic approaches, but being specific also means that the cancer needs to be dependent on the Hh pathway for it to be effective. After you read the article snippets below you should see that cancer and Hedgehog pathway activation are sometimes related to adult stem cells.


There are a few other pathways such as Wnt and BMP(s) that also lead to cancers.

Here is my fav article:

ATURE|VOL 432 | 18 NOVEMBER 2004|www.nature.com/nature

Tissue repair and stem cell renewal in carcinogenesis
Philip A. Beachy1,4, Sunil S. Karhadkar1,2 & David M. Berman2,3,4
1Department of Molecular Biology and Genetics, The Howard Hughes Medical Institute, 2Department of Pathology, 3Department of Urology and
4Department of Oncology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA


A few more articles to read

Nature. 2001 Nov 1;414(6859):105-11.
Stem cells, cancer, and cancer stem cells.

Biotechniques. 2003 Dec;35(6):1240-7.
The elements of stem cell self-renewal: a genetic perspective.

Nature. 2005 Apr 14;434(7035):843-50.
Wnt signalling in stem cells and cancer.

Recent Prog Horm Res. 2003;58:283-95.
Regulation of hematopoietic stem cell self-renewal.

#5 Hedgehog

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Posted 14 February 2008 - 12:24 AM

Very good audio casts
Bayard D. Clarkson Symposium on Stem Cells and Cancer Session
Webcasts of the Session Now Available:

* Introduction by Dr. Jane Visvader
* The stem cell niche by Dr. David T. Scadden
* Progenitor cells giving rise to cancer stem cells: Implications for treatment by Dr. Michael F. Clarke
* Cancer stem cell targeted therapy: Removing the sword Damocles by Dr. Catriona H. M. Jamieson
* Stem cells in breast carcinogenesis: Implications for prevention by Dr. Max S. Wicha


http://www.aacr.org/...er-session.aspx


Also if you think about the similarities between

ASC and Cancer Cells
  • Don't get recognized by the immune system
  • Poorly differentiated
  • Can move to different places in the body (metastasis)


#6 Mind

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Posted 04 December 2008 - 11:54 PM

Cancer Stem Cells May Not Be as Big a Factor as Originally Thought.

The controversial idea that all tumors are created by cancer stem cells received a setback Wednesday.

The theory holds that a tiny percentage of cancer cells — perhaps one in a million or one in 10,000 — are responsible for creating tumors. Like evil relatives of standard organ-forming stem cells, cancer stem cells build tumors. It's an appealing idea because it provides a new, well defined target for treatment.

But a new study casts doubt on the idea that only a few cancer cells are able to generate tumors. By tweaking the experimental design other cancer researchers had been using — the new study used a different type of mice — a highly-respected stem cell oncologist found that as many as 25 percent of melanoma cells were capable of reproducing.

What makes the study particularly surprising is that its lead author was a founder of Oncomed, the leading cancer stem cell biotech startup, and comes out of the University of Michigan, where much of the early work on cancer stem cells was conducted.

"We're not trying to claim there is no merit to the field, but we think that the frequency of cancer stem cells will be much higher," said Sean Morrison, director of the Center for Stem Cell Biology at the U-M Life Sciences Institute and coauthor of the study in Nature Thursday. "And there will be some cancers like melanoma where lots of cells will be tumorigenic and it won't be possible to treat those cancers by treating a small subset of cells."



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#7 Mind

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Posted 01 March 2009 - 02:51 PM

Since "gene switching" is in the title of this thread, I thought this might be a good place for this recent news:

Suppressing Cancer with a Master Control Gene

New work conducted by Wouter Bossuyt, Bassem Hassan, and colleagues at VIB and K. U. Leuven has tested this theory. They demonstrate that in the fruit fly, master control genes steering the specialization step inhibit tumor formation.

In collaboration with colleagues from the United States, they show that loss of one of those genes, Atonal homolog 1 (ATOH1), causes colon cancer in mice. The gene regulates the last step in the specialization to epithelial cells of the colon. Humans with colon cancer frequently have an inactivated ATOH1 gene, the researchers show.

The researchers could reactivate the gene in human colon cancer cells grown in culture. This caused the tumor cells to stop growing and commit suicide. This exciting, but preliminary, result suggests that it may be possible to switch the gene back on in living patients to target their cancers. Taking this work in the test tube and using it to develop a therapy is an exciting but complicated challenge. Therefore, more work will be required to further understand the role of ATOH1 in suppressing cancer formation.



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#8 ihatesnow

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Posted 01 March 2009 - 11:47 PM

http://news.yahoo.co...temcells_safety



Cancer Stem Cells May Not Be as Big a Factor as Originally Thought.

The controversial idea that all tumors are created by cancer stem cells received a setback Wednesday.

The theory holds that a tiny percentage of cancer cells — perhaps one in a million or one in 10,000 — are responsible for creating tumors. Like evil relatives of standard organ-forming stem cells, cancer stem cells build tumors. It's an appealing idea because it provides a new, well defined target for treatment.

But a new study casts doubt on the idea that only a few cancer cells are able to generate tumors. By tweaking the experimental design other cancer researchers had been using — the new study used a different type of mice — a highly-respected stem cell oncologist found that as many as 25 percent of melanoma cells were capable of reproducing.

What makes the study particularly surprising is that its lead author was a founder of Oncomed, the leading cancer stem cell biotech startup, and comes out of the University of Michigan, where much of the early work on cancer stem cells was conducted.

"We're not trying to claim there is no merit to the field, but we think that the frequency of cancer stem cells will be much higher," said Sean Morrison, director of the Center for Stem Cell Biology at the U-M Life Sciences Institute and coauthor of the study in Nature Thursday. "And there will be some cancers like melanoma where lots of cells will be tumorigenic and it won't be possible to treat those cancers by treating a small subset of cells."






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