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9th Honors Literature

Harrison High School STEM


Revised Activity 3.3.3 The Immortal Cells

Introduction
In this activity you will read the story of Henrietta Lacks, her family, and the doctors who created the
cell line. You will also investigate the various medical breakthroughs for which the HeLa cell line has
been responsible. Finally, you will investigate the debate surrounding the commodification, or
commercialization, of human body parts. You will discuss ownership of body parts and debate what
you should or should not be able to sell for profit.

Procedure
Part I: The Story Behind HeLa

1. Read the entire book The Immortal Life of Henrietta Lacks by Rebecca Skloot.

2. Access and read the article titled “Henrietta’s Dance” written by Rebecca Skloot and
published in the April 2000 issue of the Johns Hopkins Magazine. It is accessible on the
Internet at http://www.jhu.edu/~jhumag/0400web/01.html (Links to an external site.)Links
to an external site.

3. Access and read the Article titled “An Obsession with Culture” written by Rebecca Skloot and
published in the March 2001 issue of the University of Pittsburgh’s Pitt Magazine. It is
accessible on the Internet at: http://www.pittmag.pitt.edu/mar2001/culture.html (Links to
an external site.)Links to an external site..

4. Read the following bullets chronicling how the HeLa cell line has affected modern medicine.

 George Gey successfully cultures the first immortal human cell line using cells from
Henrietta’s cervix. It is given the name HeLa after the first two letters of Henrietta’s first
and last names. (1951)
 HeLa cells become the first living cells shipped via postal mail. (1952)
 HeLa cells were the first human cells frozen; this allowed for the close examination of cell
division.
 The Tuskegee Institute opens the first “HeLa factory,” supplying cells to laboratories and
researchers and operating as a nonprofit. Within a few years, HeLa was sold for profit.
(1952)
 Scientists use HeLa cells to help develop the polio vaccine. (1952)
 Scientists infected HeLa cells with many diseases such as mumps and measles, which
led to the creation of the modern field of virology.
 A geneticist in Texas was able to accurately calculate the number of chromosomes in a
human cell using HeLa. This eventually made it possible for doctors to diagnose
chromosomal disorders such as Down’s syndrome.(1953)
 HeLa cells become the first cells ever cloned. (1953)
 Chester Southam conducts experiments to see whether or not injections of HeLa cells
could cause cancer. (1954)
 HeLa cells were sent into space prior to any astronauts and then were included on the
first manned mission. (1960)
 HeLa cells are fused with mouse cells, creating the first animal-human hybrid cells.
(1965)
 HeLa cells allowed for advances in the field of medical ethics. After scientists injected
patients without their consent with cancer cells to discover how cancer spreads, medical
review boards and informed consent by patients were institutionalized. (1965 and 1966)
 Scientists exposed HeLa cells to radiation to better understand the effects of nuclear
radiation on human cells.
 Scientists used HeLa cells to better understand the invasiveness and infectiousness of
salmonella. (1973)
 HeLa cells were used to help uncover that the sexually transmitted virus called Human
Papilloma Virus causes cervical cancer. (1984)
 A scientist discovered the presence of an enzyme called a telomere that is used in a cell
to rebuild a cell’s telomeres. The presence of this enzyme in a cell causes cancer. (1989)
 The early cloning technology started because of HeLa cells led to isolating stem cells,
cloning entire animals, and in vitro fertilization.
 Scientists exposed HeLa cells to M. tuberculosis to learn how the disease attacks human
cells. (1993)
 Researchers used HeLa cells to test nanotechnology by injecting the cells with iron
nanowire and silica-coated nanoparticles. (2005)
 HeLa cells are used to test potential cancer drugs, such as those used to treat breast
cancer and leukemia.
 HeLa cells are used to test various products such as cosmetics, drugs, household
chemicals, viruses, and biological weapons.

5. Record any differences you find among the four sources and account for what causes the
differences. These may be differences in facts, styles, genres, etc.
1) The book The Immortal Life of Henrietta Lacks is different from the other articles, because
even though it is a non-fiction text, it is written in a narrative format instead of informational
like the 2 articles. These differences are expected because they are written for different
purposes. One article is for the Johns Hopkins Magazine and the other one is for the
University of Pittsburgh’s Pitt Magazine. The book is written for a wider audience and would
need to be longer and formatted differently to get all the information and stories into it.
2) In the article “Henrietta’s Dance”, Lawrence’s wife is named Barbra. In the book The
Immortal Life of Henrietta Lacks, her name is Bobbette. This could have been different
because oral history for the book/article could come from different sources since Rebecca
Skloot was not interviewing the family at the time of this article.
3) The bulleted list states the major findings that HeLa cells were used in creating. The book
and articles talked about the story of the cells from the beginning, like where and why they
were removed. This difference again could have been because of source differences,
intended audiences, and/or intended purposes.
4) In addition to the reason above, the book goes into more detail about the major findings that
HeLa was used for and the implication of them. The bulleted list only gives an overview of
what happened in each year. There are big gaps in years which the book filled with smaller
discoveries made.
5) The article featured in the Johns Hopkins Magazine had more detail on Henrietta’s family,
while the Pitt Magazine article focused in the scientific aspect. The book went into great
detail on both. This could be because they were meant for different people. The people at
Johns Hopkins knew Henrietta and her family, and the University of Pittsburgh didn’t. The
book told stories of the family and the scientific aspect so people reading it could understand
the importance of both parts.

Part II: Medical Ethics

6. Read the position statements in the table. Use reliable Internet websites to research each
position statement and create arguments for and against each position statement.

Position Statement Support for Position Support Against Position


People should have the The tissue is originally from Once tissues or blood
right to control what’s their body, making it their samples are taken from a
done with their tissues property. It is still their person, they are no longer
once tissues are removed genetic make-up once it has considered a part of that
from their bodies. been removed, so it is still a person since they are just a
part of them, even though it bunch of cells now. They
is not in their body. cannot grow into another
person because they are
specialized. DNA might
make up a person; however it
cannot be used to make
another person from this
small sample.
Giving patients property People like to know what Research would not be
rights of their tissues their cells are being used hindered because of this.
might hinder research for, and giving informed People can culture cells to
because fewer people consent allows that. This use and that will help be able
would allow the use of might hinder research to have more testing material
slightly because people if necessary. Some people
their tissue, restricting might not like or agree with would still donate because it
access to the necessary the research being done. would help others.
raw materials.
Tissues taken from a The issue is part of the Tissues taken from patients
patient and sold for profit patient’s body and it being are no longer part of the
should profit the individual sold. This should mean that patient’s body and therefore
or the individual’s family the patient’s body is being have no financial tie to the
from whom the tissue was sold. This should give the patient. They should not get
patient “property rights” paid for something that is not
taken.
over their own tissues. theirs.
Allowing patients to profit This would hinder scientific This would not hinder
from their tissues would progress because people scientific progress because
hinder scientific progress would try and negotiate the the prospect of money being
because patients would price of their tissues and made from the donation of
hold out for excessive samples, causing a lull in tissues or blood samples
purchase of the samples. makes it more appealing.
profits.
People would want more People would be more likely
money than necessary for to give samples if money was
their samples. involved.
People can sell their Organs are just clusters of Since selling organs is
sperm, their eggs, and cells, which is the same illegal by federal law, it
their blood. There is no thing bodily tissues are but raises the question of “if it
reason they should not be on a smaller scale. If was legal, would people
able to sell their tissues someone can sell tissues find illegal ways to get the
and organs. then why can’t they sell organs they want to sell?”.
organs? Organs are illegal to sell
for a reason; however you
can donate them to be
transplanted into people.

Conclusion
7. In your opinion, was Dr. Gey’s use of Henrietta Lacks’ cells unethical? Support your
response with evidence from all three sources.

I do think it was unethical for Dr. Gey to use Henrietta’s cells without consent. However, in
the 1950’s, it was not common for patients to be informed of what their tissues were being
used for, or if samples were even taken (Henrietta’s Dance). Had the cells not grown, there
would not be the debate of whether it was unethical because most people wouldn’t have
heard of HeLa cells.

8.
If Dr. Gey had not been able to use or to grow the cells that became the HeLa cell line, how
might medical research and health care be different now? Support your response with
evidence.

If the cell had not been “immortal”, then there could possibly be no polio vaccine or some
chemotherapy drugs (bullets 5 and 20 above). It would have taken longer to figure certain
things about cancer, such as the moment when a cell turns cancerous and the enzyme that
keeps cancer cells growing. Because of the research HeLa has been able to provide, I
believe that the world of health care and medicine would be completely different. People still
use HeLa cells to this day, which cost up to $167 (The Immortal Life of Henrietta Lacks).

9. Do you feel that the Lacks family should be compensated for the use of Henrietta’s cancer
cells for scientific study? Explain your answer.

I feel that Henrietta’s family should be compensated for their loss and the scientific
contributions of HeLa cells. If people did not feel like they should be given money for the
cells, the family could be compensated with healthcare benefits. The family deserves to be
compensated because they lost their mother/wife/cousin/ or other relative name, and were
unaware of the research and discoveries made from the cells. Hospitals and laboratories
could give the Lacks family a portion of the profit of selling the cells because they are much
more expensive now. This means there is even more of a profit gap that could be spared.

Adapted from
© 2013 Project Lead The Way, Inc.
Principles of Biomedical Science Activity 3.3.3 and Student Resource Sheet 3.3.3

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