Cancer Cells vs. Normal Cells

What is the difference between cancer cells and normal cells?

Normal cells in the body grow and divide in the way in which they should. New cells are produced only when they are needed. Cancer cells grow uncontrolled and have nothing to do with the needs of the body. A mass of tissue that forms when cells grow and are not needed, then they form what is called a tumor. There can be two different kinds of tumors in the body – benign and malignant. Benign tumors are non-cancerous and malignant tumors are cancerous.

Cancer cells are damaged normal cells. They could continue growing until they endanger healthy cells and organs of the body. They have a different growth pattern than normal cells and tend to multiply in the wrong way. Thus they can spread over a very large area and do not have the immunity that normal cells do.

While normal cells are similar in structure to cancer cells, the number of them in more balanced with the needs of the body and the activity level of the individual. They perform a purpose in the body. They have a blood supply system. They contribute to the body’s immune system and empower the body to be healthy.

There are three different classifications of cancer cells, which are expressed in grade levels.

Grade 1 cancer cells

These cells do not look any different from normal cells. They grow slowly and give little symptoms that they are cancerous. When cancer is discovered at this point it is said to be in the early stage and is curable.

Grade 2 cancer cells

At this point there is a difference in the appearance and growth of the cancer cells from normal cells. Although they are still growing, they are growing at a faster than normal rate. The cancer is still curable at this stage if the proper treatment is given. There is also the possibility that the cancer is incurable because a complete cure can only be found for Grade 1 cancers.

Grade 3 cancer cells

These cells are in the final stage of growth and are out of control. The patient is usually in a lot of pain, especially in the area of the body where the cancer cells are most numerous.

What happens when cell growth gets out of control?

The tumors that result in parts of the body from uncontrolled cell growth are classified as one of two types of growths – benign and malignant.

Benign

Sometimes cells start to grow without regard for the normal balance between cell death and the need for new cells. The growth that develops is small and harmless and is therefore called a benign tumor. It can develop in any part of the body, but it is not cancerous because it doesn’t invade or damage any other part of the body. They can be removed without risk and they are never fatal.

Malignant

Cells grow and divide regardless of the body’s needs and keep growing. They are very aggressive and the resulting growths are called malignant tumors. They are cancerous and they invade the other cells of the body so that they can spread rapidly. They can even break away and enter the blood stream, which gives them access to all parts of the body and result in new tumors.

Some forms of cancer are curable and others are not. However, in the majority of cases where the cancer cells are discovered in the early stages, the outcome is positive.

 

  • Natalie

    hiii

  • Vadim Shapoval

    Difference
    between Tumor Cells and Normal Cells. Contact inhibition is the natural process
    of arresting cell growth when two or more cells come into contact with each
    other. Contact inhibition controls cell growth by allowing cells to replicate
    as old cells die but keeps unnecessary tissues from forming in their place. Normal
    cells have their own identity and obey the rule of contact inhibition. Normal
    cells adhere to each other and expire at the end of their life cycles. Tumor cells
    typically lose these properties and thus grow in an uncontrolled manner even
    when in contact with neighboring cells. Tumor cells do not follow the rules of
    contact inhibition, adherence and self-destruction (apoptosis, programmed cell death). Usually, tumor cell contain
    faulty DNA and chromosomes (some chromosomes may be duplicated or deleted). Tumor
    cells spread through the body via the lymphatic and circulatory systems. Clearly,
    tumor cells evade the immune system. Unlike normal cells that are specialized, tumor
    cells are non-specialized and do not contribute to the functioning of a body
    part. Normal cells have specialized behaviors and serve a purpose. Tumor cells have
    lost their specialized function. The first tumor cells (in the human body) are
    not very malignant cells; subsequent (mature) tumor cells are extremely
    malignant cells. Ordinarily, old normal cells undergo apoptosis, a series of
    enzymatic reaction that lead to the death of the cell. Normal cells will
    self-destruct if genetic / chromosomal abnormalities are found. Tumor cells
    fail to undergo apoptosis. Normal cells divide about 50 times and then stop
    dividing and die. Tumor cells can enter the cell cycle repeatedly, and in this
    way, they are potentially immortal. According to the Ferromagnetic Theory of
    Cancer / Carcinogenesis / Oncogenesis / Tumorigenesis (Iron Conception), any
    tumor cells are cells with numerous intracellular superpara-, ferri- and
    ferromagnetic nanoparticles. Any normal cells are cells with non-numerous
    intracellular superpara-, ferri- and ferromagnetic nanoparticles. Any cancer
    and ALS work by these nanoparticles. Tumor cells (cells with these
    nanoparticles; excessively negatively charged cells) do not follow the rules of
    contact inhibition and adherence. Enzyme activity can be affected by these
    nanoparticles (immortality of tumor cells). The immune system does not identify these
    nanoparticles within cellular organelles (the immune system can’t distinguish
    between dia-, para-, superpara-, ferri- and ferromagnetic micro- and nano-objects).
    These nanoparticles can chaotically-anarchically distort DNA and shift
    chromosomes by local magnetic fields (mistakes in DNA; chromosomal faults;
    deformed mitoses; non-specialization and ugliness of tumor cells). Oncologists-clinicians
    must beat cancer (a subtle iron disease) by non-complicated anti-iron methods
    of The Old Testament.

    • Xena

      My Mom has ALS an is deterioting quickly. Would you explain in simple terms exactly what you would do to stop the progression of this disease?

      Your help would be much appreciated.
      Thank you
      Shirley

      • Vadim Shapoval

        Xena! You must read the Ferromagnetic Theory of ALS. ALS is money of ALS-researchers. ALS-researchers can’t beat money. ALS-researchers invent false ALS-researches. Vadim Shapoval

  • http://profile.yahoo.com/2SHGP6CKFM2RXLQRNTPNNMMNCE Vadim

    Any malignant tumor cells are cells with numerous intracellular superpara-, ferri- and ferromagnetic nanoparticles. Any benign tumor cells are cells with non-numerous intracellular superpara-, ferri- and ferromagnetic nanoparticles. Any normal cells are cells almost without intracellular superpara-, ferri- and ferromagnetic nanoparticles. VS Pages gives three different classifications of cancer cells, which are expressed in grade levels. See: ‘Iron Chelators for Cancer Therapy and Ferromagnetic Theory of Cancer’.
    Observations that rapid neoplastic cell proliferation requires iron
    have led to the understanding that some iron chelators may be useful
    against cancer. Researchers endeavor to develop more effective iron
    chelators for cancer therapy. Chelation
    is a very effective way to treat heavy-metal poisoning. Since
    the 1970s, iron chelation therapy (the
    removal of excess iron from the body with special drugs) has
    been used as an alternative to regular phlebotomy to treat excess
    iron stores in people with hemochromatosis. The goal of iron
    chelation therapy is to prevent iron-mediated injury to cells.
    Researchers can’t beat cancer by iron
    chelators because: 1) researchers invent ultra-complicated iron
    chelators; 2) researchers mix anti-cancer iron chelation therapy with
    chemotherapy and radiation therapy. According to the Ferromagnetic
    Theory-2006 of Cancer (Iron Conception), any tumor cells are cells
    with numerous intracellular superpara-, ferri- and ferromagnetic
    nanoparticles (any normal cells are cells with non-numerous
    intracellular superpara-, ferri- and ferromagnetic nanoparticles).
    Researchers must beat cancer (a subtle iron disease) by
    non-complicated iron chelators of The Old Testament: 1) intratumoral
    injections [sulfur (2%) + olive oil (98%); 36.6C – 39.0C] (by
    ceramic needles) [suppression of tumors and large metastases]; 2)
    accurate slow blood loss (even 75%) [hemoglobin control]
    (neutralization of micro-metastases); 3) goat’s milk diet and
    anti-iron drinking water containing hydrogen sulfide (neutralization
    of micro-metastases.

  • Vadim Shapoval

    Cancer, ALS, AIDS, Religious Beliefs of Patients and Medicine-2013. Scientists can’t beat cancer, ALS and AIDS. Cancer has a reputation as a deadly disease. ALS is a devastating and fatal neurological disorder. Since the beginning of the epidemic, nearly 30 million people have died from AIDS-related causes. Scientists ignore iron-cancer, iron-ALS and iron-AIDS scientific data. In the past, scientists ignored scientific ‘antibiotic data’. In 1871-1872 V. Manassein and A. Polotebnov used antibiotic properties of fungi (green or blue molds on decaying food). In 1928 Alexander Fleming discovered penicillin. It became widely used during World War II. Howard Florey and Ernst Chain took up Fleming’s research and found a way to purify penicillin. Chemotherapy of virus diseases is an extremely interesting but, at the same time, a very difficult problem. At present, there are no effective therapeutic agents for the treatment of many virus infections. Chemotherapy of malignant tumors, like that of virus diseases, presents considerable difficulties because the difference between the metabolism of tumor cells and that of normal cells is negligible. All types of tissues and cells of the macro-organism may undergo malignant degeneration, which makes difficult the search for drugs that would have a selective effect on the tumor tissues and would not affect the healthy ones. Scientists ignore information: a human organism can survive ‘accurate anti-iron aggression'; cancer, ALS and HIV/AIDS can’t survive ‘accurate anti-iron aggression’. All forms of cancer are caused by intracellular superpara-ferri-ferromagnetic ‘infection’. All forms of ALS are caused by intraneuronal superpara-ferri-ferromagnetic ‘infection’. Any somatic cell / any neuron should be interpreted as a society of dia-, para-, superpara-, ferri- and ferromagnetic nanoparticles. Enzyme systems of any virus contain heme iron and non-heme iron. Deficiency of iron destabilizes enzyme systems of any virus. Slow blood loss (even 75%) [hemoglobin control], goat’s milk diet and drinking water containing hydrogen sulfide can gradually neutralize intracellular / intraneuronal superpara-ferri-ferromagnetic nanoparticles and enzyme systems of HIV. Any micrometastases and isolated tumor cells will weaken. Moreover, according to the Ferromagnetic Cancer Theory (Theory from The Old Testament; Iron Conception), ceramic needles can enter solution [sulfur (2%) + olive oil (98%); 36.6C - 39.0C] to tumors and large metastases, ‘individuals with mutilated DNA’, who live within religious and non-religious cancer patients. Medicine-2013 will beat cancer, ALS and HIV/AIDS by non-complicated anti-iron methods of The Old Testament. http://www.medicalnewstoday.com/opinions/103745/  ;  VS Pages & Shapoval http://vspages.com/cancer-cells-vs-normal-cells-1420/