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Untitled - D Ank Unlimited

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oncogene 541 one-turn recombination signal sequence<br />

α Surface antigen<br />

(AFP) is demonstrable in approximately 70% of hepatocellular<br />

carcinomas.<br />

oncogene<br />

A gene linked to carcinogenesis when deregulated. Such<br />

genes may encode positive regulators of cell growth. They<br />

may be activated by mutation or retroviral integration. They<br />

are involved in the control of cell growth and when defective<br />

in structure or expression can lead to abnormal cell<br />

proliferation resulting in tumor generation. Genes with the<br />

capacity to induce neoplastic transformation of cells, they<br />

are derived from normal genes (proto-oncogenes) or from<br />

oncogenic RNA (oncorna) viruses. Their protein products<br />

are critical for the regulation of gene expression and growth<br />

signal transduction. Translocation, gene amplification, and<br />

point mutation may lead to neoplastic transformation of<br />

proto-oncogenes. Oncogenes may be revealed through the<br />

use of viruses that induce tumors in animals or by derivation<br />

of tumor-causing genes from cancer cells. The human<br />

genome has more than 20 proto-oncogenes and cellular<br />

oncogenes. An oncogene alone cannot produce cancer. It<br />

must be accompanied by malignant transformation involving<br />

multiple genetic steps. Oncogenes encode four types of<br />

proteins, including growth factors, receptors, intracellular<br />

transducers, and nuclear transcription factors.<br />

oncogenesis<br />

The process by which tumors develop.<br />

oncogene theory<br />

A concept of carcinogenesis that assigns tumor development<br />

to latent retroviral gene activation through irradiation<br />

RNA<br />

virus<br />

DNA<br />

virus<br />

Embryonic cell<br />

(gene α is functional)<br />

α Gene<br />

Infected<br />

cell<br />

RNA<br />

provirus<br />

α Gene<br />

repressed<br />

Normal adult cell<br />

(repressed α gene)<br />

Oncofetal antigen.<br />

Oncogenic virus.<br />

α Surface antigen<br />

Malignant adult cell<br />

(de-repressed α gene)<br />

α Gene<br />

De-repressed<br />

or carcinogens. These retroviral genes are considered to<br />

be normal constituents of cells. Following activation, these<br />

oncogenes are presumed to govern the neoplasm through<br />

synthesized hormones and even the possible construction<br />

of a complete oncogenic virus. This concept states that all<br />

cells may potentially become malignant.<br />

oncogenic virus<br />

Any virus, whether DNA or RNA, that can induce malignant<br />

transformation of cells. An example of a DNA virus is<br />

human papillomavirus. Retroviruses are RNA viruses.<br />

oncomouse<br />

Commercially developed transgenic mice into which<br />

human genes have been introduced to make the mice more<br />

susceptible to neoplasia. Transgenic mice are used for both<br />

medical and pharmaceutical research.<br />

one gene, one enzyme theory (historical)<br />

An early hypothesis that proposed that one gene encodes one<br />

enzyme or other protein. Although basically true, it is now<br />

known that one gene encodes a single polypeptide chain, and<br />

it is necessary to splice out mRNA introns composed of junk<br />

DNA before mRNA can be translated into a protein.<br />

one-hit theory<br />

A concept related to complement activation that states that<br />

only a single site of preparation is necessary for red cell<br />

lysis during complement-antibody-mediated injury to a cell<br />

membrane.<br />

one-turn recombination signal sequence<br />

Immunoglobulin gene recombination signal sequence separated<br />

by an intervening sequence of 12 base pairs.<br />

Steady state<br />

Integrated<br />

Infectious RNA<br />

virus and cell membrane<br />

Tumor-specific<br />

transplantation antigen<br />

Leukemia<br />

Virus-specific antigen<br />

Malignancy<br />

O

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