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Untitled - D Ank Unlimited

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tumor necrosis factor (TNF) receptors 723 TUNEL-based assays<br />

Type I<br />

COOH<br />

Type II<br />

COOH<br />

TNF receptors designated type I (CD120a) and type II (CD120b). Both the<br />

55-kDa type I and the 75-kDa type II receptors bind TNF-α and TNF-β<br />

(lymphotoxin). These receptors belong to the NGRF/TNFR superfamily.<br />

Their extracellular domains contain four cysteine-rich repeats.<br />

tumor necrosis factor (TNF) receptors<br />

A receptor for tumor necrosis factor composed of 461amino<br />

acid residues and an extracellular domain that is rich<br />

in cysteine. Cell surface receptors for TNF-α and TNF-β<br />

(LTα) are expressed by most cell types. Of the two TNF<br />

receptors, TNF-RI mediates most biologic effects of TNF-N<br />

(TNF-RII). TNF receptors possess cysteine-rich extracellular<br />

motifs that include Fas and CD40. These receptors<br />

have essentially no homology in their intracellular domains.<br />

Tumor virus<br />

particle<br />

Tumor cell<br />

Tumor-specific antigens (TSAS).* Each tumor induced by a<br />

single virus will express the same TSA on the cell<br />

surface despite the morphology of the cell.<br />

Soluble types I and II have been described in urine and<br />

serum. With the exception of erythrocytes and resting<br />

T cells, TNF receptors are found on most types of cells.<br />

Whereas the type I p55 receptor is widely distributed on<br />

various cell types, the type II p75 receptor appears confined<br />

to hematopoietic cells. The human p55 receptor contains<br />

three potential N-linked glycosylation sites; the type II p75<br />

form contains only two.<br />

tumor promoter<br />

Refer to phorbol esters.<br />

tumor regression<br />

A decrease in size or remission of a malignant tumor as a<br />

consequence of anticancer therapy; regression may occur<br />

spontaneously without treatment.<br />

tumor rejection antigen<br />

An antigen that is detectable when transplanted tumor cells<br />

are rejected; also called tumor transplant antigen.<br />

tumor-specific antigen (TSA)<br />

An antigen present on tumor cells but not found on normal<br />

cells. Murine tumor-specific antigens can induce transplantation<br />

rejection in mice. Encoded by mutated cellular genes<br />

or viral oncogenes.<br />

tumor-specific determinants<br />

Epitopes present on tumor cells and also identifiable in<br />

varying quantities and forms on normal cells.<br />

tumor-specific transplantation antigen (TSTA)<br />

Epitopes that induce rejection of tumors transplanted<br />

among syngeneic (histocompatible) animals.<br />

tumor suppressor genes<br />

Genes such as p53 and PTEN that encode cellular proteins<br />

that prevent cells from becoming neoplastic; their absence<br />

promotes carcinogenesis.<br />

TUNEL assay (TdT-dependent dUTP–biotin<br />

nick end labeling)<br />

A technique that identifies apoptotic cells in situ by fragmentation<br />

of their DNA. Immunohistochemical staining<br />

with enzyme-linked streptavidin identifies biotin-tagged<br />

dUTP added to the free 3′ ends of the DNA fragments by<br />

the terminal deoxynucleotidyl transferase (TdT) enzyme.<br />

TUNEL-based assays<br />

DNA fragments can be stained in situ by using terminal<br />

deoxynucleotidyl transferase (TdT) to polymerize labeled<br />

nucleotides onto the ends of nicked DNA (TdT-dependent<br />

Tumor-<br />

specific<br />

antigen<br />

(TSA)*<br />

T

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