Column A Column B a. tumor-associated 1. more resistant to antigens chemotherapy and radiation than tumor cells b. peptide splicing 2. novel peptide antigens arising from viruses, genomic and protein alterations, aberrant MRNA splicing, and peptide splicing c. cancer stem cells 3. formation of peptide bonds in the proteasome producing a non-contiguous amino acid sequence not found in the |native protein | 4. arise from reactivation of normally silenced genes or overexpression of genes d. soluble MIC glycoproteins e. tumor-specific antigens 5. enhance removal of NKG2D from lymphocyte surfaces

Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Question

Match the term in column A with its description in column B.

Column A
Column B
a. tumor-associated 1. more resistant to
antigens
chemotherapy and radiation
than tumor cells
b. peptide splicing
2. novel peptide antigens arising
from viruses, genomic and
protein alterations, aberrant
MRNA splicing, and peptide
splicing
c. cancer stem cells 3. formation of peptide bonds in
the proteasome producing a
non-contiguous amino acid
sequence not found in the
|native protein
| 4. arise from reactivation of
normally silenced genes or
overexpression of genes
d. soluble MIC
glycoproteins
e. tumor-specific
antigens
5. enhance removal of NKG2D
from lymphocyte surfaces
Transcribed Image Text:Column A Column B a. tumor-associated 1. more resistant to antigens chemotherapy and radiation than tumor cells b. peptide splicing 2. novel peptide antigens arising from viruses, genomic and protein alterations, aberrant MRNA splicing, and peptide splicing c. cancer stem cells 3. formation of peptide bonds in the proteasome producing a non-contiguous amino acid sequence not found in the |native protein | 4. arise from reactivation of normally silenced genes or overexpression of genes d. soluble MIC glycoproteins e. tumor-specific antigens 5. enhance removal of NKG2D from lymphocyte surfaces
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