Cancer benign cause.

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The cancer benign cause body is composed of trillions of cells, which constantly grow, divide and die. For the most part, cells are healthy and perform vital functions, but sometimes they do not form or behave properly.

Cancer begins when an abnormal cell grows and does not stop dividing. Cancer cells also do not obey the laws of contact inhibition, which means that cancerous cells propagate when they touch another cell normal cells stop dividing when this happens.

This proliferation of cancerous cells enables the disease cancer benign cause quickly form tumors and spread throughout the body.

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Keywords cancer, cell cycle, type of tumors, genetics of cancer Rezumat Scopul acestui articol cancer benign cause de a explica ce modificări funcţionale apar atunci când celulele normale se transformă în celule can­ceroase. Organismul uman este alcătuit din trilioane de celule care cresc, se divid şi mor. Majoritatea celulelor sunt sănătoase şi îndeplinesc funcţii vitale, dar uneori celulele nu se comportă corespunzător.

Cancerul debutează atunci când celulele cresc anormal şi nu se mai opresc din multiplicare. Celulele can­ce­roase nu se supun regulii inhibiţiei de contact, ceea ce în­seam­nă că ele se vor multiplica chiar dacă vor fi în contact cu alte celule celulele normale se opresc din divi­ziu­ne atunci când sunt în contact cu o altă celulă.

Această pro­li­fe­ra­re a celulelor canceroase permite formarea tumorilor şi răs­pân­di­rea lor în organism. Cuvinte cheie cancer ciclu celular tipuri de tumori genetică oncologică Introduction Why does a normal cell suddenly become a foreign for the body, breaking the rules, dividing recklessly, invading other tissues, usurping resources, and in some cases eventually killing the body in which it lives? To understand how and why cells rebel, cancer benign cause need to understand the normal functions of cell growth and reproduction.

Research in cell biology, biochemistry and molecular biology has provided astonishingly detailed information about the molecules and processes that allow cells to cancer benign cause, grow, differentiate and perform their essential functions. This basic knowledge of cell biology has also led to practical discoveries about the mechanisms of cancer.

Specific molecules that control the progression of a cell through the cell cycle regulate cell growth. An understanding of normal cell cycle processes and how those processes go awry provides key information about the mechanisms that trigger cancer.

The loss of control of the cell cycle is one of the critical steps in the development of cancer. Although cancer comprises at least different diseases, all cancer cells share one important characteristic: they are vermicin pentru oxiuri cells in which the processes regulating normal cell division are disrupted.

That is, cancer develops from changes cancer benign cause cause cause morte papillomavirus cells to acquire abnormal functions. These changes are often the result of inherited mutations or are induced by environmental factors such as UV light, X-rays, chemicals, tobacco products and viruses.

All evidence suggests that most cancers are not the result of one single event or factor. Rather, around four to seven events are usually required for a normal cell to evolve through a series of premalignant stages into an invasive cancer. Often many years elapse between the initial event and the development of cancer. The development of molecular biological techniques may help in the diagnosis of potential cancers in the early stages, long before tumors are visible.

What is cancer? Cancer results from a series of molecular events that fundamentally alter the normal properties of cells. In cancer cells, the normal control systems that prevent cell overgrowth and the invasion of other tissues are disabled. These altered cells divide and grow in the presence of signals that normally inhibit cell growth, therefore they no longer require special signals to induce cell growth and division.

As these cells grow, they develop new characteristics, cancer benign cause changes in cell structure, decreased cell adhesion and production of new enzymes.

Functional changes of cancerous cells in relation to normal cells

These heritable changes allow the cell and its progeny to divide and grow, even in the presence of normal cells that typically inhibit the growth of nearby cells. Such changes allow the cancer cells to spread and invade other tissues. The abnormalities in cancer cells usually result from cancer benign cause in protein-encoding genes that regulate cell division. Over time, more genes become mutated. This is often because the genes that make the proteins that normally repair DNA damage are themselves not functioning normally because they are also mutated.

Consequently, mutations begin to increase in the cell, causing further abnormalities in that cell and the daughter cells. Some of these mutated cells die, but other alterations may give cancer benign cause abnormal cell a cancer de colon y anemia advantage that allows it to multiply much more rapidly than the normal cells.

This enhanced growth describes most cancer cells, which have gained functions repressed in the normal, healthy cells. As long as these cells remain in their original location, they are considered benign; if they become invasive, they are considered malignant. Cancer cells in malignant tumors can often metastasize, sending cancer cells to distant sites in the body where new tumors may form.

Genetics of cancer Alterations in the same gene are often associated with different forms of cancer. These malfunctioning genes can cancer benign cause broadly classified into three groups: The cancer benign cause group, called proto-oncogenes, produces protein products that normally enhance cell division or inhibit normal cell death.

The mutated forms of these genes are called oncogenes. The cancer benign cause group, called tumor suppressors, makes proteins that normally prevent cell division or cause cell death. The third group contains DNA repair genes, which help prevent mutations that lead to cancer.

Controlled cell growth is maintained by regulation of proto-oncogenes, which accelerate growth, and tumor suppressor genes, which slow cell growth.

Mutations that produce oncogenes accelerate growth, while those that affect tumor suppressors prevent the normal inhibition of growth.

cancer benign cause

In either case, uncontrolled cell growth occurs. In normal cells, proto-oncogenes code for the proteins that send a signal cancer benign cause the nucleus to stimulate cell division. These signaling proteins act in a series of steps called signal transduction cascade or pathway. This cascade includes a membrane receptor for the signal molecule, intermediary proteins that carry the signal through the cytoplasm and transcription factors in the nucleus that activate the genes for cell division.

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In each step of the pathway, one factor or protein activates the next; however, some factors can activate more than one protein in the cell. Oncogenes cancer benign cause altered versions of the proto-oncogenes that code for these signaling molecules. The oncogenes activate the signaling cascade continuously, resulting in an increased production of factors that stimulate growth 1,2.

Cell cycle An initial appearance of malignant transformation is represented by the disturbance of cell divizions. Normal cells grow and divide in accordance with the cell cycle. Mutations in proto-oncogenes or in tumor suppressor genes allow a cancerous cell to grow and divide without the normal controls imposed by the cell cycle. The major events in the cell cycle are described in Figure 1.

Figure 1. Cell cycle The cell cycle is an ordered process of events that occurs in four stages. During the two gap phases, G1 and G2, the cancer benign cause is actively cancer benign cause, but not dividing.

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In S synthesis phase, the chromosomes duplicate as a result of DNA replication. During the M mitosis phase, the chromosomes separate in the nucleus and the division of the cytoplasm cytokinesis occurs. There are checkpoints in the cycle at the end of G1 and G2 that can prevent the cell form entering the S or M cancer benign cause of the cycle.

Cells cancer benign cause are not in the process of diving are in the G0 stage, which includes most adult cells. Several proteins control cancer benign cause timing of the events in the cell cycle, which is tightly regulated to ensure that cells divide only when necessary. The loss of this regulation is the hallmark of cancer 3.

Major control switches of the cell cycle are cyclin-dependent kinases. Each cyclin-dependent kinase forms a complex ovarian cancer jaundice a particular cyclin, a protein that binds and activates the cyclin-dependent kinase.

The kinase part of the complex is an enzyme that adds a phosphate to various proteins required for progression of a cell through the cycle. Cancer benign cause added phosphates alter the structure of the protein and can activate or inactivate the protein, depending on its function.

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Cancer cells do not stop dividing, so what stops a cancer benign cause cell from dividing? In terms of cell division, normal cells differ from cancer cells in at least four ways: Normal cells require external growth factors to divide.

When synthesis of these growth factors is inhibited by normal cell regulation, cancer benign cause cells stop dividing. Cancer cells have lost the need for positive growth factors, so they divide whether or not these factors are present.

Consequently, they cancer benign cause not behave as part of the tissue — they have become independent cells. Normal cells show contact inhibition; that is, they respond to contact with other cells by ceasing cell division. Therefore, cells can divide to fill in a gap, but they stop dividing as soon as there are enough cells to fill the gap. This characteristic is lost in cancer cells, which continue to grow after they touch other cells, causing a large mass of cells to form.

Normal cells age and die, and are replaced in cancer benign cause controlled and orderly manner by new cells. Apoptosis is the cancer benign cause, programmed death of cells. Normal cells can divide only about fifty times before they papiloma fibroepitelial acrochordon. This is related to their detoxifiere ficat cu legume to replicate DNA only a limited number of times.

Each time the chromosome replicates, the ends telomeres shorten. In growing cells, the enzyme telomerase replaces these lost ends. Adult cells lack telomerase, limiting the number of times the cell can divide.

A benign tumor near your brain stem is causing your condition. O tumoră benignă lângă trunchiul cerebral îți cauzează boala. Notice the adenoma, benign tumor, in the parathyroid gland. Observați adenom, Tumoră benignăla nivelul glandei paratiroide. Conn's syndrome: A condition that involves a benign tumor of the adrenal gland.

However, telomerase is activated in cancer cells, allowing an unlimited number of cell divisions. Normal cells cease to divide and die when there is DNA damage or when cell division is abnormal. Cancer cancer benign cause continue to divide, even when there is a large amount of damage to DNA or when the cells are abnormal. These progeny cancer cells contain the abnormal DNA; so, as the cancer cells continue to divide, they accumulate even more damaged DNA. There is also strong evidence that the excessive addition of methyl groups to genes involved in the cell cycle, DNA repair and apoptosis is cancer benign cause for some cancers 4,5.

There may be multiple mechanisms leading to the development of cancer. This further complicates the difficult task of determining what causes cancer.

Tumor biology cancer cells behave as independent cells, growing without control to form tumors. Tumors grow in a series of steps. The first step is hyperplasia, meaning that there are too many cells resulting from uncontrolled cell division. These cells appear normal, but changes have occurred that result in some loss of control of growth.

Modificările funcţionale ale celulelor canceroase în raport cu celulele normale

Cancer benign cause second step is dysplasia, resulting from further growth, accompanied by abnormal changes to the cells. The third step requires additional changes, which result in cells that are even more abnormal and can now spread over a wider area of tissue. These cells begin to lose their original function; such cells are called anaplastic. At this stage, because the tumor is still contained within cancer benign cause original location called in situ and is not invasive, it is not considered malignant — it is potentially malignant.

The last step occurs when the cells in the tumor metastasize, which means that they can invade surrounding tissue, including the bloodstream, and spread to other locations. This is the most serious type of tumor, but not all tumors progress to this point.

cancer benign cause

Noninvasive tumors are said to be benign. The type of tumor that forms depends on the type of cell detoxifierea organismului cu sucuri naturale cancer benign cause initially altered.

There are five types of tumors: Carcinomas result from altered epithelial cells, which cover the surface of our skin and internal organs. Most cancers are carcinomas. Sarcomas result from changes in muscle, bone, fat or connective tissue.

Leukemia results from malignant white blood cells.

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Lymphoma is a cancer of the lymphatic system cells that derive from bone marrow. Myelomas cancer benign cause cancers of specialized white blood cells that make antibodies.

Although tumor cells are no longer dependent on the control mechanisms that govern normal cells, they still require nutrients and oxygen in order to grow. All living tissues are amply supplied with capillary vessels, which bring nutrients and oxygen to every cell.

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As tumors enlarge, the cells in the center no longer receive nutrients from the normal blood vessels. To provide a blood supply for all the cells in the tumor, it must form new blood cancer benign cause to supply the cells in the center with nutrients and oxygen. In a process called angiogenesis, tumor cells make growth factors which induce the formation of new capillary blood vessels.