How do the original cancer cells in a human body start?

How do the original cancer cells in a human body start?

Answer by Robert Weinberg, PhD- a founding member of the Whitehead Institute for Biomedical Research and the Daniel K. Ludwig Professor for Cancer Research at Massachusetts Institute of Technology (MIT) ). He is also the first Director of the Ludwig Cancer Center at MIT.

As mentioned in a previous answer (http://talkabouthealth.com/how-do-cancer-cells-grow-and-replicate-so-quickly-do-they-reproduce-from-themselves-or-somehow-change-normal-cells-to-cancer-cells), cancer cells arise from normal cells in which damaged genetic information accumulates that perturbs the behavior of these cells. For example, when a smoker inhales, the mutagenic chemicals in the cigarette smoke damage genes in lung cells, and these cells, which now carry damaged genes including oncogenes, now begin to proliferate uncontrollably, leading years later to a lung cancer.

Is it true that metastatic disease has likely started to spread well before detection of the primary tumor? Is it too late to be treated at this point?

Is it true that metastatic disease has likely started to spread well before detection of the primary tumor? Is it too late to be treated at this point?

Answer by Robert Weinberg, PhD- a founding member of the Whitehead Institute for Biomedical Research and the Daniel K. Ludwig Professor for Cancer Research atMassachusetts Institute of Technology (MIT) ). He is also the first Director of the Ludwig Cancer Center at MIT.

A: It is true that cancer cells often spread and generate metastases long before the primary tumor has been detected. So, even if one wipes out the primary tumor, there is always the danger that metastatic tumor colonies survive and begin to grow and threaten the survival of the person from whom a primary tumor has been removed. However, there is some hope: certain types of treatments that are in current use that succeed in eliminating primary tumors may also have effects on eliminating disseminated cancer cells, and thus eliminating metastases!

His webpage:http://www.wi.mit.edu/research/faculty/weinberg.html

Robert Weinberg, PhD Founding member of the Whitehead Institute for Biomedical Research and the Daniel K. Ludwig Professor for Cancer Research at the Massachusetts Institute of Technology (MIT) is answering cancer genetics questions today.

Robert Weinberg, PhD:

Dr. Weinberg is a founding member of the Whitehead Institute for Biomedical Research and the Daniel K. Ludwig Professor for Cancer Research at the Massachusetts Institute of Technology (MIT). He is also the first Director of the Ludwig Cancer Center at MIT. He is an internationally recognized authority on the genetic basis of human cancer.

Dr. Weinberg and his colleagues isolated the first human cancer-causing gene, the ras oncogene, and the first known tumor suppressor gene, Rb, the retinoblastoma gene. The principal goal of his research program is to determine how oncogenes, their normal counterparts (proto-oncogenes), and tumor suppressor genes fit together in the complex circuitry that controls cell growth. More recently, his group has succeeded in creating the first genetically defined human cancer cells. He is particularly interested in applying this knowledge to improve the diagnosis and treatment of breast cancer.

His lab now primarily focuses on two areas: the interactions between epithelial and stromal cells (the two major types of cells found in mammalian tissue) that produce carcinomas and the processes by which cancer cells invade and metastasize.

Epithelial and stromal cells. Many mammalian tissues are formed from distinct epithelial and stromal cell layers. Often, a tumor that forms in an epithelial tissue layer must recruit stromal cells in order to become a carcinoma. Weinberg’s lab is exploring the molecular process by which this recruitment occurs. In addition, his lab has been investigating a signaling pathway operating within epithelial cells that enables them to release signals that stimulate blood vessel growth in nearby stromal cells.

Invasion and metastasis. Weinberg’s lab is focusing on a small group of transcription factors—proteins that control gene expression. These proteins, which are typically involved in embryogenesis, may contribute to cancer cells’ ability to disseminate to distant sites in the body where they may form metastases. Weinberg and his team are examining mechanisms by which tumors can reactivate the properties of these proteins that are active during embryonic development and exploit these transcription factors to execute various steps of the “invasion-metastasis” cascade—the sequence of steps that enables primary tumor cells to disseminate through the body and seed cancer cells. Additionally, the scientists are studying the role of cancer stem cells—the self-renewing, tumor-seeding cells that have been found in a number of solid tumors in the past few years. In 2008, Weinberg lab investigators reported a finding that brings together these two research themes: cancer cells induced to follow one of these embryonic pathways gain many of the properties of adult stem cells.

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