Molecular Basis of Neoplasia - Nelson Flashcards

1
Q

What is the key difference between benign and malignant neoplasms

A

Benign neoplasms cannot spread to other tissues and malignant neoplasms have th capability to metastasize

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2
Q

What four types of mutations cause cancer?

A

1) Growth-promoting proto-oncogenes
2) Growth-inhibiting tumor supressor genes
3) Genes that regulate apoptosis
4) Genes involved in DNA repair

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3
Q

1) Self-sufficiency in Growth Signals

A

Proliferate without external stimuli, usually a consequence of proto-oncogene activation (need to lose only one allele)

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4
Q

2) Insensitivity to growth-inhibitory signals

A

Inactivation of tumor suppressor genes (need to lose both alleles)

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5
Q

3) Altered cellular metabolism

A

Aerobic Glycolysis (the Warberg effect)

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6
Q

4) Evasion of apoptosis

A

Resistant to programmed cell death via upregulation of Bcl-2

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7
Q

5) Limitless replicative potential

A

Immortality (a stem-cell like property)

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8
Q

6) Sustained angiogenesis

A

Tumor growth necessity

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9
Q

7) Ability to invade and metastasize

A

Processes that are intrinsic to the tumor cells and signals that are initiated from the tissue environment

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10
Q

8) Ability to evade host immune response

A

These are the 8 hallmarks of cancer

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11
Q

Define Oncogene

A

Mutated, overexpressed proto-oncogene

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12
Q

Define Oncoprotein

A

Mutated protein that can’t be regulated

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13
Q

Define Tumor Supressor Gene

A

Inhibits cellular proliferation and prevents cell growth; regulates cell cycle, transcription and cellular differentiation; both alleles need to be mutated

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14
Q

Define Proto-oncogene

A

Only one allele needs to be mutated to cause uncontrolled cell growth and proliferation

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15
Q

Describe the Warburg Effect

A

Cancer cells use aerobic glycolysis as a form of cellular respiration characterized by high glucose uptaek and increased conversion of glucose to lactose (fermentation)

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16
Q

Describe the Molecular Classification of Cancer

A

Classification of cancer according to therapeutic targets rather than cells of origin and morphology