Back To Basics | Jackson Free Press | Jackson, MS

Back To Basics

This week, the Democratic Congress is likely to pass expanded federal funding for embryonic stem-cell research, although President George W. Bush will almost certainly veto the bill. The Republican Congress passed similar legislation this summer, but President Bush used the first veto of his administration to kill that bill last September.

Although we have long heard fantastic descriptions of all that stem cells might do to save human life, few members of the public are familiar with how far stem-cell research has come.

In the last two years, researchers have made startling discoveries about the role stem cells play in cancer. In fact, scientists now believe that malfunctioning stem cells are responsible for many cancers, including leukemia, breast cancer, brain cancer, prostate cancer and colon cancer, among others.

The reason stem cells play this role is that most of the cells in our body are regularly replaced. Your skin is completely replaced every month, the lining of your gut every two weeks and the platelets in your blood every 10 days. Most cells in your body are born to die in weeks, and they can only divide so many times. Stem cells, by contrast, last all your life, and they can divide without limit. Every part of your body was born of a stem cell.

The body operates this way to protect us from cancer. If all cells in your body reproduced like stem cells, then a mutation in any one of them might lead to cancer. Because most cells are restricted in how they divide, however, an individual cell might become "cancerous" only to die after a few divisions.

The problem is when stem cells suffer mutations. Instead of acting as the source of new cells to replenish your body, cancerous stem cells become the source of tumors, breeding generation after generation of cancer cells. Even if doctors remove or kill all visible traces of a cancerous tumor, missing just one stem cell could lead to a relapse, which is one reason why cancer that seems eradicated can return.

What's more, new research published in the journal Nature this September indicates that stem cells may hold the key to understanding how and why we age. As stem cells age, the chances that they will accumulate cancer-causing mutations grows. This is the underside to how stem cells protect us—most cells die before their mutations can cause disease, but stem cells live as long as we do. After decades of life, it is almost inevitable that stem cells will become damaged by free radicals and other mutagens. (See this issue's cover story for examples of how free radicals and other mutagens are boosting levels of cancer.)

The body's response is to slow down stem cells as we age, reducing how often they divide. This helps to protect us from cancer, but it also means that our tissues deteriorate because they are no longer replenished by new, young cells from our stem cells. Our skin becomes papery and our organs frail. The alternative: rampant cancer. About 40 percent of people will develop some form of cancer at some point, usually in old age. Colon cancer is the third most common form, but the average age of people who develop colon cancer is 70.

If we want to understand cancer, we must understand stem cells. If we want to understand aging, we must understand stem cells.

In 2001, President Bush limited federally funded research to 60 stem-cell lines, though only a handful of those were viable. Since then, researchers have discovered that the lines Bush approved were contaminated by the mouse "feeder cells" used to nurture the cells, making them worthless for use in human therapy.

Scientists have tried to sidestep controversy by developing stem-cell lines from another source, such as umbilical or amniotic fluid, and social conservatives have twittered over the potential of the amniotic variety. Yet, even the scientists who discovered these cells do not claim that they have the same potency as embryonic stem cells, and their research has not yet been duplicated by other scientists.

The only reason scientists have bothered with amniotic fluid at all is that some people think harvesting stem cells from a handful of the 400,000 unused embryos stored in fertility clinics is murder. Social conservatives claim that every embryo is a person, and even though fertility clinics are going to throw away every embryo, using any of them to understand human disease is a crime.

When President Bush vetoed the stem cell bill this September, he surrounded himself with "snowflake" children—that is, children who came from frozen embryos, embryos that were "adopted" by evangelicals. He did not mention that only 128 embryos out of 400,000 have been adopted.

As we are battered by sermons about the sanctity of life, it's easy to forget that calling an embryo a person is only a metaphor. That's why few women have adopted frozen embryos—there are so many actual children who need our care and love. An embryo does not go hungry. An embryo does not scream in soiled diapers. We know real people when we see them.

Morality is more than conviction—morality requires wisdom, and wisdom abhors hypocrisy. If the 400,000 frozen embryos in our country are truly people, then fertility treatments should be illegal, as they produce so many "people" doomed to die. But embryos are not people, and the reason why social conservatives have not tried to ban fertilization treatments is that most people just won't do that to a couple who are desperate to bring new life into the world.

That is, people won't vote to ban fertility treatments because they know that one actual child means more than a thousand "potential" children, just as they know that real morality means real people. Cells in a frozen tank aren't children, and stern speeches about the Lord's wrath are not the Lord's word.

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