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WAR ON CANCER

Cancer is an unqualified enemy of the living world costing both in emotional turmoil and in 
thousands of careers invested in diagnosis, treatment, and research. Cancer is a broad collection 
of molecular disease states characterized by cells that divide in an uncontrolled fashion and that 
no longer respect their role or confinement within their tissue of origin. Despite the many 
environmental, hereditary, viral, dietary, and chemical causes of cancer, they all have one 
common root cause: mutational changes in genes that control cell division. What is the scientific 
community doing to attempt to eliminate the most common forms of cancer that are ravaging 
society?
INSTRUCTIONS
 Read the course text chapter 8 sections 8.1-8.4 on cell division, then specifically the last 
section (8.6) on how cells become cancerous. This is the context for completing the War 
on Cancer Assignment.
 Watch the Presentation “Ways to Fight Cancer.” Notice that the presentation outlines 
essentially 3 approaches to fighting cancer: a) reduction of cancer risks, b) correction of 
cancer genes, and c) destruction of cancerous tissue.
 Open the “War on Cancer – 10 Discoveries” document. Study the discoveries. Then, 
open the assignment submission link in the text box and number from 1 to 10. 
 Reflect carefully on discovery 1. Would this discovery be more useful for a) reducing 
cancer risks, b) correcting/restoring cancer cells to normal, or c) destroying cancerous 
tissue? After number 1 in your list, place the letter representing the approach to fighting 
cancer that would best be served by this new discovery. Place only 1 letter for each 
number. (More than 1 approach may be served, but which one is most likely to be helped 
most significantly?)
 Repeat this analysis for each of the remaining 9 discoveries. Return to the “Ways to Fight 
Cancer” presentation as needed for additional perspective. When finished, your 
assignment should be a numbered (1-10) list of letters (a), (b) or (c).

 

 

 

 

 

 

WAR ON CANCER: 10 DISCOVERIES
1. Malignant brain tumors in adults are fast-growing cancers with median survival rates of 15 
months, even with aggressive treatment. Researchers have been searching for genetic 
“signatures” (characteristic groups of cancer-causing genes) that could help in defining the 
kind of brain tumor the patient has. They hope to be better able to predict the course of the 
disease and more accurately design the patient’s course of treatment.
2. Immunologists are working with a mutation (HER2) that is expressed on the surface of 
many breasts, bladder, pancreatic, and ovarian cancer cells. They have made antibodies 
against this mutant surface protein. These antibodies have been covalently bonded to a 
“gene expression vector” that makes cells light up when incubated with luciferin from 
fireflies. The vector takes the gene for luciferin into the cancer cells. The researchers have 
shown that their antibody can accurately find and “light up” cancer cells. Their next step is 
to bond the antibody to an expression vector that carries the normal HER2 gene into 
mutant cancer cells.
3. Virologists are modifying lentiviruses as vectors for carrying proto-oncogenes into cancer-
transformed cells in culture. They are developing this virus for inserting the ras proto-
oncogene directly into its correct location in the genome. The correct ras gene will already 
be linked to human DNA on either side of it and complexed with a recombination enzyme 
that will insert it into its correct location within the human genome. At the same time, the 
recombination enzyme will excise the defective oncogenic form of ras. The cells in 
culture should again come under normal hormonal control and require extra-cellular 
signals in order to continue dividing.
4. Organic chemists are exploring structural variations of the organic compound avobenzone 
(1-[4-Methoxyphenyl]-3-[4-tert-butylphenyl] propane-1,3-dione) for inclusion in sunblock 
products. Avobenzone is known for its ability to absorb a broad spectrum of ultra-violet 
radiations including UVB light (known to enhance the frequency of basal cell and 
squamous cell carcinomas [skin cancers]); and UVA rays thought to increase the 
frequency of melanoma cancers. New variations in the structure of avobenzone are hoped 
to retain the ability to absorb harmful UV radiation while having an increased stability in 
the presence of that radiation.
5. Tobacco smoking is the leading cause of preventable deaths worldwide. It is a risk factor 
for lung cancer and several other types of cancer. Results of analysis of the entire human 
gene collection (the “genome”) support some previous findings that a region of human 
chromosome number 15 contains one or more genes that are associated with smoking 
intensity (the number of cigarettes smoked per day) and the closely related trait of nicotine 
dependency. Lung cancer associated with smoking Scanning people’s genomes for these 
genes will help them to determine their risk of addiction should they begin smoking 
tobacco.
6. Immunologists are investigating ways to destroy lymphocytes (white blood cells of the 
immune system) that have become cancerous (lymphomas). A current drug Rituxamab

 

 

 

BIOL 101
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contains antibodies that bind to the surfaces of these lymphocytes setting them up for 
destruction by the cancer patient’s own immune system. They are currently seeking ways 
to modify the antibody’s structure so that it will attract the cancer patient’s “natural killer” 
(NK) cells to the lymphocytes. Success of this project will bring a multi-faceted immune 
response against lymphomas and hasten destruction.
7. Molecular biologists have developed a new sequence of human genes called an ankyrin 
insulator sequence. A new corrected or therapeutic gene is placed within this sequence. Its 
role is to make an active area on a human chromosome where the new gene can work 
efficiently no matter what chromosome it lands on.
8. Biochemists are analyzing the many, many components of red meat (beef and pork) to 
determine which component, if any, will cause increased colorectal cancer rates in mice 
when the component is administered orally. Studies have shown that higher colorectal 
cancer rates in humans are associated with higher consumption rates of red meat.
9. Molecular biologists have taken nanoparticle-sized spheres and used them to deliver a 
cell-killing toxin from bee venom to tumors in mice, substantially reducing tumor growth 
without harming normal body tissues. Nanoparticles are known to concentrate in solid 
tumors because blood vessels in tumors show “enhanced permeability and retention 
effect” or EPR. Hence substances such as nanoparticles escape more readily from the 
bloodstream into tumors and the generally poor drainage of lymph from tumors further 
helps trap the particles in tumor tissue.
10. Biochemists have discovered a protein kinase enzyme named BRAF that is an important 
link in a molecular pathway that causes a cell to divide. Normally, BRAF responds to 
signals coming from outside the cell—signals calling for the cell to divide normally under 
normal conditions. But there is a mutation in BRAF enzymes that causes it to activate the 
cell toward division continually. In this way it gives rise to melanomas and thyroid or 
ovarian cancers. Biochemists have also found a drug, vemurafenib, which binds 
selectively to mutant BRAF totally inactivating it. Cells that have inactivated BRAF 
undergo apoptosis—a process that leads to cell death.

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