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© Cengage Learning 2015
11.5 What Happens When Control Over
the Cell Cycle Is Lost?
• Types of mutations that affect cell cycle:
– Checkpoint genes mutate causing the loss-of-
function of their protein products
– Controls that regulate checkpoint gene
expression fail
• Cell makes either too much or too little of gene
product
1
© Cengage Learning 2015
The Role of Mutations (cont’d.)
• When enough checkpoint mechanisms
fail, a cell loses control over its cell cycle
– Interphase may be skipped, so division occurs
over and over with no resting period
– Signaling mechanisms that cause abnormal
cells to die may stop working
2
© Cengage Learning 2015
The Role of Mutations (cont’d.)
• Neoplasm: accumulation of abnormally
dividing cells
• Tumor: neoplasm that forms a lump
• Oncogene: gene that helps transform a
normal cell into a tumor cell
3
© Cengage Learning 2015
The Role of Mutations (cont’d.)
• Proto-oncogenes: gene that, by mutation,
can become an oncogene
– Example: growth factors – molecules that
stimulate mitosis and differentiation
– Most neoplasms carry mutations resulting in
an overactivity or overabundance of the
epidermal growth factor (EGF) receptor
4
© Cengage Learning 2015
The Role of Mutations (cont’d.)
5
© Cengage Learning 2015
The Role of Mutations (cont’d.)
• Checkpoint gene products that inhibit
mitosis are called tumor suppressors
– Tumors form when checkpoint gene products
are missing
– Examples:
• Tumor cells often have mutations in the BRCA1
and BRCA2 checkpoint genes
• HPV (human papillomavirus) cause cells to make
proteins that interfere with tumor suppressors
6
© Cengage Learning 2015
The Role of Mutations (cont’d.)
7
A B
© Cengage Learning 2015
Cancer
• Benign neoplasms such as warts are not
usually dangerous
– Slow growth
– Cells retain plasma membrane adhesion
proteins
8
© Cengage Learning 2015
Cancer (cont’d.)
• A malignant neoplasm get progressively
worse and is dangerous to health
• Characteristics of malignant cells:
– Abnormal growth and development
– Altered cytoplasm and plasma membrane
– Cells undergo metastasis: process in which
malignant cells spread from one part of the
body to another
9
© Cengage Learning 2015
Cancer (cont’d.)
10
3
4
1 2
© Cengage Learning 2015
Cancer (cont’d.)
• Cancer: disease that occurs when a
malignant neoplasm physically and
metabolically disrupts body tissues
– Each year, cancer causes 15 to 20 percent of
all human deaths in developed countries
11
© Cengage Learning 2015
Cancer (cont’d.)
• Mutations in multiple checkpoint genes are
required to transform a normal cell into a
malignant one
– Such mutations may take a lifetime to
accumulate
12
© Cengage Learning 2015
Cancer (cont’d.)
• Lifestyle choices can reduce one’s risk of
acquiring mutations:
– Do not smoke
– Avoid sun exposure
13
© Cengage Learning 2015
Cancer (cont’d.)
• Some neoplasms can be detected with
periodic screening such as gynecology or
dermatology exams
– If detected early enough, many types of
malignant neoplasms can be removed before
metastasis occurs
14
© Cengage Learning 2015
Cancer (cont’d.)
15
A Basal cell carcinoma
is the most common
type of skin cancer. This
slow-growing, raised
lump may be uncolored,
reddishbrown, or black.
B Squamous cell carci-
noma is the second
most
common form of skin
cancer. This pink
growth,
firm to the touch, grows
under the surface of
skin.C Melanoma spreads
fastest. Cells form dark,
encrusted lumps that
may itch or bleed easily.

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11.5

  • 1. © Cengage Learning 2015 11.5 What Happens When Control Over the Cell Cycle Is Lost? • Types of mutations that affect cell cycle: – Checkpoint genes mutate causing the loss-of- function of their protein products – Controls that regulate checkpoint gene expression fail • Cell makes either too much or too little of gene product 1
  • 2. © Cengage Learning 2015 The Role of Mutations (cont’d.) • When enough checkpoint mechanisms fail, a cell loses control over its cell cycle – Interphase may be skipped, so division occurs over and over with no resting period – Signaling mechanisms that cause abnormal cells to die may stop working 2
  • 3. © Cengage Learning 2015 The Role of Mutations (cont’d.) • Neoplasm: accumulation of abnormally dividing cells • Tumor: neoplasm that forms a lump • Oncogene: gene that helps transform a normal cell into a tumor cell 3
  • 4. © Cengage Learning 2015 The Role of Mutations (cont’d.) • Proto-oncogenes: gene that, by mutation, can become an oncogene – Example: growth factors – molecules that stimulate mitosis and differentiation – Most neoplasms carry mutations resulting in an overactivity or overabundance of the epidermal growth factor (EGF) receptor 4
  • 5. © Cengage Learning 2015 The Role of Mutations (cont’d.) 5
  • 6. © Cengage Learning 2015 The Role of Mutations (cont’d.) • Checkpoint gene products that inhibit mitosis are called tumor suppressors – Tumors form when checkpoint gene products are missing – Examples: • Tumor cells often have mutations in the BRCA1 and BRCA2 checkpoint genes • HPV (human papillomavirus) cause cells to make proteins that interfere with tumor suppressors 6
  • 7. © Cengage Learning 2015 The Role of Mutations (cont’d.) 7 A B
  • 8. © Cengage Learning 2015 Cancer • Benign neoplasms such as warts are not usually dangerous – Slow growth – Cells retain plasma membrane adhesion proteins 8
  • 9. © Cengage Learning 2015 Cancer (cont’d.) • A malignant neoplasm get progressively worse and is dangerous to health • Characteristics of malignant cells: – Abnormal growth and development – Altered cytoplasm and plasma membrane – Cells undergo metastasis: process in which malignant cells spread from one part of the body to another 9
  • 10. © Cengage Learning 2015 Cancer (cont’d.) 10 3 4 1 2
  • 11. © Cengage Learning 2015 Cancer (cont’d.) • Cancer: disease that occurs when a malignant neoplasm physically and metabolically disrupts body tissues – Each year, cancer causes 15 to 20 percent of all human deaths in developed countries 11
  • 12. © Cengage Learning 2015 Cancer (cont’d.) • Mutations in multiple checkpoint genes are required to transform a normal cell into a malignant one – Such mutations may take a lifetime to accumulate 12
  • 13. © Cengage Learning 2015 Cancer (cont’d.) • Lifestyle choices can reduce one’s risk of acquiring mutations: – Do not smoke – Avoid sun exposure 13
  • 14. © Cengage Learning 2015 Cancer (cont’d.) • Some neoplasms can be detected with periodic screening such as gynecology or dermatology exams – If detected early enough, many types of malignant neoplasms can be removed before metastasis occurs 14
  • 15. © Cengage Learning 2015 Cancer (cont’d.) 15 A Basal cell carcinoma is the most common type of skin cancer. This slow-growing, raised lump may be uncolored, reddishbrown, or black. B Squamous cell carci- noma is the second most common form of skin cancer. This pink growth, firm to the touch, grows under the surface of skin.C Melanoma spreads fastest. Cells form dark, encrusted lumps that may itch or bleed easily.

Notas do Editor

  1. Figure 11.8 Effects of an oncogene. In this section of human breast tissue, a brown-colored tracer shows the active form of the EGF receptor. Normal cells are lighter in color. The dark cells have an overactive EGF receptor that is constantly stimulating mitosis; these cells have formed a neoplasm.
  2. Figure 11.9 Checkpoint genes in action. Radiation damaged the DNA inside this nucleus. Two proteins have clustered around the same chromosome breaks in the same nucleus; both function to recruit DNA repair enzymes. The integrated action of these and other checkpoint gene products blocks mitosis until the DNA breaks are fixed. A Red dots show the location of the BRCA1 gene product. B Green dots pinpoint the location of another checkpoint gene product.
  3. Figure 11.10 {Animated} Neoplasms and malignancy. 1 Benign neoplasms grow slowly and stay in their home tissue. 2 Cells of a malignant neoplasm can break away from their home tissue. 3 The malignant cells become attached to the wall of a lymph vessel or blood vessel (as shown here). They release digestive enzymes that create an opening in the wall, then enter the vessel. 4 The cells creep or tumble along inside vessels, then exit the same way they got in. Migrating cells may start growing in other tissues, a process called metastasis.
  4. Figure 11.11 Skin cancer can be detected with early screening.