Cancer Stem Cells: The Main Cause Of Cancer

(22) In this context of subclinical mutational carriers, individual patient genetic, epigenetic and immunological variables that govern full acquisition of malignant potential are expected to have predictive and therapeutic implications. In addition, investigation of clonal adaptive processes especially those associated with pre-MDS/MDS transition could facilitate understanding of disease pathogenesis.

Cancer is a genetic disease caused by certain changes to genes that control the way our cells function, especially how they grow and divide. Genes carry the instructions to make proteins, which do much of the work in our cells. Certain gene changes can cause cells to evade normal growth controls and become cancer. Genetic changes that promote cancer can be inherited from our parents if the changes are present in germ cells, which are the reproductive cells of the body (eggs and sperm). Such changes, called germline changes, are found in every cell of the offspring. In general, cancer cells have more genetic changes than normal cells. But each person’s cancer has a unique combination of genetic alterations.

Cancer is described as the abnormal growth of cells. Normal cells are replaced with abnormal cells in which their deoxyribonucleic acid (DNA) has been damaged or augmented (McCance & Huether, 2014). Cancer cells with their various DNA changes are characterized by growing uncontrollably, being immortal with an unlimited lifespan

Breast Cancer is a type of cancer where in the breast cells growth are uncontrolled. To enhance our understanding of breast cancer, knowing how any cancer can develop is crucial. Cancer develops as a result of the alteration of the genes, or abnormal changes in the genes accountable for managing the growth of the cells and maintaining their health. In each nucleus, the genes operates as the “control room.” The cells in our bodies replace themselves through a process called cell growth in which the

Cancer is a disease caused by an uncontrolled division of abnormal cells. The DNA sequence in cells can be changed as a result of copying errors during replication. If these changes whatever their cause are left uncorrected, both growing and non-growing somatic cells might gain many mutations that they could no longer function. The relevance of DNA damage and repair to the generation of cancer was obvious when it was recognized that everything that causes cancer also cause a change in the DNA sequence. Tumor suppressor genes are protective genes and normally they limit cell growth by monitoring the speed of cell division, repair mismatched DNA and control when a cell dies. When a tumor suppressor gene is mutated cells grow

cancer stem cell: current controversies and new insights” National Institutes of Health (995) December 5, 2005]

When cells in the body start dividing and regenerating uncontrollably, they lead to cancer – and this is true for all the cells in the body. If the cancer is not nipped in its bud early on, it can spread to other parts of the body. This presents the common question asked regards cancer; how can it be stopped early on? The same can be said for cancers that start from the bone marrow such as multiple myelomas.

Many scientists believe that embryonic stem cell (ESC) research is the key to curing diseases such as cancer and HIV. Stem cells are so important to biomedical research because they are primitive cells that are capable of replicating indefinitely producing a multitude of different types of cells. This means that one of these pre-determined cells has to potential of becoming any range of over two hundred tissues with epithelial cells to blood and

Human life starts from a fertilized cell which breaks down, again and again, an adult human body is composed of the abundance of cells and each one have their own specific function to perform. During adulthood, most of the cell does not duplicate except some cells continue to divide to replace the old or damaged cell in blood, skin and intestine. This growth is very controlled and no excessive cell growth takes place. But sometimes when a mutation occurs in one or more genes which causes unnecessary cell reproduction and as a conclusion, there is no control over the growth of cells. It is called malignant transformation and this is the starting of cancer (Hosick et al., 2015). There are many different types of cancer but the early stage diagnosis

Besides fetal stem cells, adult stem cells are also researched for new therapies yet are not as effective. According to the National Institutes of Health (2015), the stem cells obtained from an embryo are analyzed in order “to identify how undifferentiated stem cells become the differentiated cells that form the tissues and organs.” Many diseases are caused by an abnormality of cell division and cause the body to decline in health over time. The most common disease of abnormal cell growth is cancer, which destroy body tissues. Although there are

The normal process of cell division is altered in cancerous cells typically by mutations in the genes involved in the regulation of cellular division. The number of mutations normally will begin to spread because when the genes that make DNA repairing proteins become mutated, this causes the DNA that they would be repairing to become mutated as well. Some changes allow the damaged cells to divide more quickly than normal and to invade other tissues. The cancers cells can divide even where there are signals and normal cells meant to prevent the cell growth.

The body is made up of hundreds of millions of living cells. Normal body cells grow, divide, and die in an orderly fashion. During the early years of a person’s life, normal cells divide faster to allow the person to grow. After the person becomes an adult, most cells divide only to replace worn-out or dying cells or to repair injuries. Cancer begins when cells in a part of the body start to grow out of control. There are many kinds of cancer, but they all start because of out-of-control growth of abnormal cell (American Cancer Society, 2010).

First, we must understand what cancer is and how it forms, cancer is “a malignant and invasive growth or tumor, especially one originating in epithelium, tending to recur after excision and to metastasize to other sites.”1 it is when normal cells mutate and begin to reproduce at such an accelerated rate that body does not have time to get rid of these bad cells and a mass begins to grow creating a problem for the body.

The concept of neurogenesis being confined to the embryonic stage became less obvious with the onset of discovery of neural stem cells maintained in two distinct regions of the mammalian adult brain namely dentate gyrus (DG) of the hippocampus and the sub ventricular zone (SVZ) of the forebrain lateral ventricles14,18,19. What makes these neural stem cells a more credible target for oncogenic transformation? The continual presence of undifferentiated, mitotically active, self renewable stem cells at the apex of the hierarchy bundled in discrete germinal niches in the mammalian brain throughout the lifespan of an organism allows them to accumulate mutations, thus rendering them vulnerable for neoplastic reprogramming. There has been increasing evidence that the genetic and epigenetic mechanisms that initiate and maintain the NSC developmental state are possibly deregulated in GB to emerge as Glioma initiating cells or Brain tumor stem cells20. The discovery of BTSC has high clinical significance in the neuro-oncology field, as evidenced by major diverse roles it plays in various aspects of tumor growth such as tumor initiation, maintenance, progression, angiogenesis and tumor recurrence owing to therapeutic resistance, some of which are described

Cancer occurrs by the production of multiple mutations in a single cell that causes it to proliferate out of control. Cancer cells often different from their normal neighbors by a host of specific phenotypic changes, such as rapid division rate, invasion of new cellular territories, high metabolic rate, and altered shape. Some of those mutations may be transmitted from the parents through the germ line. Others arise de novo in the somatic cell lineage of a particular cell. Cancer-promoting mutations can be identified in a variety of ways. They can be cloned and studied to learn how they can be controlled.