Week 8: Questions Flashcards
What is the leading cause of death in Canada? What percentage of Canadians die from this cause?
Cancer is the leading cause of death in Canada with 28.2% of all deaths
What are the most common types of cancer in Canada (except for non-melanoma skin cancer)?
Prostate cancer with 20%, lung cancer with 13%, breast cancer with 25% and colorectal cancer with 10%
What percentage of Canadians will develop cancer during their lifetime?
44% of men and 43% of woman
What percentage of Canadians diagnosed with lung cancer are still alive five years after diagnosis? What are the percentages for breast cancer and prostate cancer?
For lung cancer, it is low at 22%, prostate is 91% and breast is 89%
Distinguish between a benign and a malignant tumor.
Benign: harmless, doesn’t spread or continue to grow
Malignant: cell growth that continues in an uncontrolled manner, resulting in cancer
Define the terms metastasis and angiogenesis. Explain why a cancerous tumor that displays these processes may be harmful or deadly.
Metastasis: When individual cancer cells leave a tumor, enter the bloodstream and develop tumors at new sites.
Full Process:
1. A small tumor is confined to its place of origin
2. Tumor cells break through the basal lamina, which is a fibrous boundary layer
3. Tumor cells invade local blood vessels
4. Tumor cells travel through the bloodstream to other places in the body
5. Tumors cells adhere in new locations, forming new tumors
Angiogenesis: successful tumors secrete chemical signals that cause blood vessels to sporut from the circulatory system - results in heavy cells receiving less oxygen and good molecules
- Successful tumors secrete chemical signals
- Chemical signals initiate the growth of blood vessels
- Blood vessels connect tumors to the blood supply, resulting in tumor growth
How Do Cancer Cells Differ from Normal Cells?
Normal:
Communicate with one another using chemical signals (division, migration, differentiation and specialization)
Have special morphologies or shapes
Attach to other cells in orderly manner to form tissues and organs
Stop dividing at certain density
Cancer:
Do not behave in orderly manner sine they are damaged
Ignore chemical signals
Do not stop dividing
Lose characteristics unique to the tissue (tumor initialized in lung will feature cells that don’t look or function like lung cells)
Lose physical connection to tissue or organ and secrete enzymes called proteases that break down other cells
Cancer cells are immortal. Explain why this is so.
Cancer cells multiply even after they reach a certain density, as a concequence, they pile up on top of eachother
There is also no limit of how many times they can divide so they are really immortal.
What is the role of growth factors?
Many normal cells require signal molecules that are called growth factors in order to grow.
They also respond to another type of signal molecule which is called a growth inhibitor which prevents cell division
In general, a growth factor is a signal molecule that enables normal cells to divide.
Cells divide, differentiate, or die. What is cell differentiation?
Cells divide to produce two identical daughter cells. Cells stop dividing to specialize in structure and function, a process called differentiation. Once differentiated, some cells may divide again under certain conditions.
In general, what is the purpose of a checkpoint in the cell cycle?
Specialized proteins called “cell cycle regulators” or “checkpoint proteins” regulate the progression from one phase of the cell cycle to the next.
The progression through these checkpoints is a strictly regulated process that usually works without errors.
When errors do occur, they can have catastrophic consequences, including the development of cancer.
Apoptosis is programmed cell death, in which normal cells die if their DNA is damaged or if they have reached the end of their life span. Cancer cells do not die on schedule, even if they are damaged or old. What are the consequences of the failure of normal cells to undergo apoptosis?
If regular cells do not undergo apoptosis, it may lead to uncontrolled cell division and subsequently lead to the development of a tumor.
G1
G1:
Phase Events & Checkpoint items
First Gap Phase: The newly divided cell enters this phase right after completing cell division (or mitosis). During G1, the cell increases in size and prepares to replicate its DNA
G1-Checkpoint: Rest or Divide?
Toward the end of G1, the cell has to be sufficiently healthy to replicate its DNA. If the DNA is undamaged and enough resources are available for the cell to keep growing and divide, growth signals will stimulate the cell to proceed to the DNA synthesis, or S, phase. Otherwise, either the cell dies or it enters a resting state, also referred to as G0 phase.
Checklist summary:
✓ No DNA damage
✓ Sufficient resources
S:
Phase Events & Checkpoint Items
Synthesis Phase: The cell replicates its DNA. At the end of this phase, the cell has two complete sets of chromosomes.
S-Checkpoint: DNA OK?
Throughout the S phase, DNA is continuously monitored for replication errors. If DNA synthesis progresses without errors, growth signals will stimulate the cell to proceed to G2, during which the cell matures.
Checklist summary:
✓ No errors during DNA replication
G2:
Phase Events & Checkpoint Items
Second Gap Phase: The cell continues to grow and prepares for division.
G2-Checkpoint: Fully Equipped?
To proceed to the next phase, all chromosomes have to be fully replicated and contain no other types of damage. Only then can it enter mitosis, or M phase, and divide.
Checklist summary:
✓ DNA without damage
✓ Chromosome set complete
✓ Enough cell components
M:
Phase Events & Checkpoint Item
Mitosis: In this last phase of the cell cycle, the cell stops growing and divides into two daughter cells, each with the same number of chromosomes.
M-Checkpoint: Are Any Sister Chromatids Unattached?
For mitosis to proceed correctly, the two copies in a duplicated chromosome (each called a sister chromatid) should both be attached to the mitotic spindle. If they are, mitosis continues: The two sister chromatids separate, becoming two chromosomes. The two identical sets of chromosomes move to opposite ends of the dividing cell.
Checklist summary:
✓ All sister chromatids attached to mitotic spindle
What would happen if the cell continued through the cell cycle after failing one of the checkpoint items?
Failures in these checkpoints could lead to the accumulation of damage, which may lead to mutations.
When errors do occur, they can have catastrophic consequences, including the development of cancer.
Make sure that you understand the difference between proto-oncogenes and oncogenes and can explain why cancer cells result from several mutations, in which one tumor suppressor gene is disabled and several oncogenes are activated.
Proto-oncogene: A gene that encodes for a protein that regulates cell division
Oncogene: A gene that tells the cell to divide in the absence of normal instructions to do so
Tumor Supressor: A gene that encodes for a protein that tells a cell not to divide
- Cancer cells result from an accumulation of several mutations
- Atleast one tumor suppressor must be disabled and severeal oncogenes activated
- In cancer cells, proto-oncogenes and tumor supressor genes are not balanced