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Stem cell ethical debate
Stem cell ethical debate
Morals and ethics surrounding stem cells
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The use of Henrietta Lacks cells has led to many scientific breakthroughs, e.g., the cure to polio, cloning, and the human genome project. Henrietta Lacks was an African American woman who died of cervical cancer in 1951. These cells underwent a mutation that caused them to become immortal, meaning that they continue to divide since her death in 1951 to this very day. However, her cells raise an ethical question, because before she died she did not give consent for scientists to use her cells and after she died they did not tell her family that they were using them. This has been an ongoing controversy because the cells have been so beneficial for society, but they are derived from shady procedures. The reason way Henrietta’s cells, HeLa cells, didn’t undergo apoptosis was that they were cancerous cells that replicated indefinitely and these cells were modified to be even more resistant due to other diseases Ms. Lacks had.
There are still many unknowns to the cause of an immortal cell line, but scientists do know it correlates with a mutation within the cell. In the case of Henrietta, the cells that were taken from her came from a tumor she had. These cells were place in vitro and began to divide endlessly and rapidly. The reason why the cells divided so rapidly was that Henrietta also had HPV and syphilis, which could have made the cells even stronger. The more prevalent question is why did her cells continue to divide after she had died? This question still has some gray areas, but scientists have a very good understanding on this topic. When the cells were kept in ideal conditions they continued to divide because just like cancerous cells the cells regulatory system malfunctions and apoptosis does not occur. In regular cells,...
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Works Cited
Anderson, Jessica Cumberbatch. "Henrietta Lacks' Family, Feds Reach Settlement On Use Of DNA Info." The Huffington Post. TheHuffingtonPost.com, 07 Aug. 2013. Web. 14 May 2014.
Andrews, Paul D. "Five Reasons Henrietta Lacks Is the Most Important Woman in Medical History." Popular Science. Bonnier, n.d. Web. 14 May 2014.
Cartwell, Alan. "Immortal HeLa Cells." Immortal HeLa Cells. Rense, 17 Feb. 2010. Web. 15 May 2014.
Freeman, Shanna. "How HeLa Cells Work." HowStuffWorks. HowStuffWorks.com, 10 Sept. 2012. Web. 15 May 2014.
Silver, Marc. "A New Chapter in the Immortal Life of Henrietta Lacks." National Geographic. National Geographic Society, 16 Aug. 2013. Web. 15 May 2014.
Skloot, Rebecca. "Rebecca Skloot Journalist, Teacher, Author of The Immortal Life of Henrietta Lacks." Rebecca Skloot FAQ Comments. Being Wicked, n.d. Web. 15 May 2014.
The book The Immortal Life of Henrietta Lacks by Rebecca Skloot is the result of years of research done by Skloot on an African American woman with cervical cancer named Henrietta Lacks. Cells from Lacks’ tumor are taken and experimented on without her knowledge. These cells, known as HeLa cells, are the first immortal human cells ever grown. The topic of HeLa cells is at the center of abundant controversial debates. Despite the fact that her cells are regarded as, “one of the most important advancements in the last hundred years” (4), little is actually known about the woman behind the cells. Skloot sets out on a mission to change this fact and share the story of the woman from whom the cells originate and her family as they deal with the effects these cells have on them.
In the book, The Immortal Life of Henrietta Lacks, by Rebecca Skloot, the author highlights the scientific advances of HeLa cells, as well as the personal setbacks of Henrietta Lacks’ family. HeLa is a commonly used cell line in laboratories worldwide and is so often referred to as “the cell line that changed modern science”. This line of immortal cells has helped advance science in ways beyond compare. HeLa has allowed cell testing, cell cloning, and the discovery of various vaccines, including the HPV vaccine. While HeLa has done wonders in the medical field, it has caused unrepairable damage among the Lacks family.
An abstraction can be defined as something that only exists as an idea. People are considered abstractions when they are dehumanized, forgotten about, or segregated and discriminated against. The scientific community and the media treated Henrietta Lacks and her family as abstractions in several ways including; forgetting the person behind HeLa cells, giving sub-par health care compared to Caucasians, and not giving reparations to the Lacks family. On the other hand, Rebecca Skloot offers a different perspective that is shown throughout the book. Rebecca Skloot’s book The Immortal Life of Henrietta Lacks describes the trials and tribulations the Lacks family has gone through because of HeLa cells and shows how seeing a person as an abstraction is a dangerous thing.
Henrietta’s cells were being inaugurated with space travel, infused into rat cells, and even being used to make infertile hens fertile again. However, these are only a few of the many accomplishments that Henrietta’s immortal cells made possible: “The National Cancer Institute was using various cells, including HeLa, to screen more than thirty thousand chemicals and plant extracts, which would yield several of today’s most widely used and effective chemotherapy drugs, including Vincristine and Taxol,”(pg.139). This example of logos from the text again shows just how important these Henrietta’s cells were to the future developments in
All I can say is amazing information of your glorious and late Henrietta Lacks. This incedible women bettered our society in ways no common human could understand at the time because of how complex this matter was and still very much indeed is. I know there is much contraversy with the matter of how scientists achived immortal cells from your late relative, and I do strongly agree with the fact that it was wrong for these researches to take advantage of this incredible women, but I know it is not for me to say nonethless it must be said that even though it was wrong to take Lacks’ cells when she was dying sometimes one must suffer to bring joy to the entire world.
The Immortal Life of Henrietta Lacks by: Rebecca Skloot has a lot of themes, but one that is most relevant in my opinion is the racial politics of medicine. Throughout the chapters, there were examples of how Henrietta, being African American, prevented her from receiving the same treatment as the white woman sitting right next to her in the waiting room. The story begins with Henrietta going to Johns Hopkins Hospital and asking a physician to check a “knot on her womb.” Skloot describes that Henrietta had been having pain around that area for about a year, and talked about it with her family, but did not do anything until the pains got intolerable. The doctor near her house had checked if she had syphilis, but it came back negative, and he recommended her to go to John Hopkins, a known university hospital that was the only hospital in the area that would treat African American patients during the era of Jim Crow. It was a long commute, but they had no choice. Patient records detail some of her prior history and provide readers with background knowledge: Henrietta was one of ten siblings, having six or seven years of schooling, five children of her own, and a past of declining medical treatments. The odd thing was that she did not follow up on upcoming clinic visits. The tests discovered a purple lump on the cervix about the size of a nickel. Dr. Howard Jones took a sample around the tissue and sent it to the laboratory.
Rebecca Skloot has done a marvelous job telling the story of Henrietta Lacks; the woman who changed science!
In 1951, the sickness of a poor African American woman named Henrietta Lacks -also know as HeLa- would go on to change the face of scientific research; without her consent. Henrietta Lacks went into John Hopkins Hospital in hopes of medical treatment, but instead her cells were unlawfully stolen from her and used for scientific advances in the world of medicine for the creations of the polio vaccine, cell cloning, vitro fertilization, and gene mapping. Long after Henrietta's death, Henrietta's family was forced to live a life of poverty without medical insurance simply because they could not afford it although their mothers cells had yielded billions of dollars due to its advances in the medical world. The scientific community and the media
To have something stolen from you is devastating and can change your life. But what if what was taken from you will save billions of human lives? In the book The Immortal Life of Henrietta Lacks by Rebecca Skloot, we see a woman named Henrietta had a biopsy of a cancerous tumor, and the cells from the tumor were able to live and grow outside of her body; and even better, the cells go on to find the cure for diseases such as polio. The catch is this: she signed a document giving her hospital permission to perform any medical procedure they find necessary to help her treatment, but she never gave specific permission for the cells in that biopsy to be tested and cultured. Now the big debate is over whether or not it was legal for her doctors
It was her cells that became what is known as HELA cells or immortal cells. Her story is interesting to me because of her impact on the science community. Her cells allowed scientist to perform
Henrietta Lacks is not a common household name, yet in the scientific and medical world it has become one of the most important and talked names of the century. Up until the time that this book was written, very few people knew of Henrietta Lacks and how her cells contributed to modern science, but Rebecca Skloot aimed to change this. Eventually Skloot was able to reach Henrietta’s remaining family and through them she was able to tell the story of not only the importance of the HeLa cells but also Henrietta’s life.
Rebecca Skloot’s novel, The Immortal Life of Henrietta Lacks, depicts the violation of medical ethics from the patient and researcher perspectives specifically when race, poverty, and lack of medical education are factors. The novel takes place in the southern United States in 1951. Henrietta Lacks is born in a poor rural town, Clover, but eventually moves to urban Turner Station. She was diagnosed and treated for cervical cancer at Johns Hopkins hospital where cells was unknowingly taken from her and used for scientific research. Rebecca Skloot describes this when she writes, “But first—though no one had told Henrietta that TeLinde was collecting sample or asked she wanted to be a donor—Wharton picked up a sharp knife and shaved two dime-sized pieces of tissue from Henrietta's cervix: one from her tumor, and one from the healthy cervical tissue nearby. Then he placed the samples in a glass dish” (33). The simple act of taking cells, which the physicians did not even think twice about, caused decades
The book The Immortal Life of Henrietta Lacks by Rebecca Skloot, was a nonfiction story about the life of Henrietta Lacks, who died of cervical cancer in 1951. Henrietta did not know that her doctor took a sample of her cancer cells a few months before she died. “Henrietta cells that called HeLa were the first immortal human cells ever grown in a laboratory” (Skloot 22). In fact, the cells from her cervix are the most important advances in medical research. Rebecca was interested to write this story because she was anxious with the story of HeLa cells. When she was in biology class, her professor named Donald Defler gave a lecture about cells. Defler tells the story about Henrietta Lacks and HeLa cells. However, the professor ended his lecture when he said that Henrietta Lacks was a black woman. In this book, Rebecca wants to tell the truth about the story of Henrietta Lacks during her medical process and the rights for Henrietta’s family after she died.
Henrietta Lacks was born on August 18, 1920 in Roanoke, Virginia. She stayed with her grandfather who also took care of her other cousins, one in particular whose name is David (Day) Lacks. As Henrietta grew up, she lived with both her Grandpa Tommy and Day and worked on his farm. Considering how Henrietta and Day were together from their childhood, it was no surprise that they started having kids and soon enough got married. As the years continued, Henrietta noticed that she kept feeling like there was a lump in her womb/cervix and discovered that there was a lump in her cervix. Soon enough, Henrietta went to Johns Hopkins Medical Center to get this check and learned that she had cervical cancer. But here is where the problem arises, Henrietta gave full consent for her cancer treatment at Hopkins, but she never gave consent for the extraction and use of her cells. During her first treatment TeLinde, the doctor treating Henrietta, removed 2 sample tissues: one from her tumor and one from healthy cervical tissue, and then proceeded to treat Henrietta, all the while no one knowing that Hopkins had obtained tissue samples from Henrietta without her consent. These samples were later handed to ...
The Immortal life of Henrietta Lacks by Rebecca Skloot is a story of science, religion and the life of the Henrietta Lacks herself. It has won many awards and was on the New York Best Seller list for over three years. To summarize it briefly, the book is based on the cells of Henrietta Lacks who died of cervical cancer in 1951. Sometime before she died, some of her tissue was sampled and used for research without her permission. They used the cells form her body to experiment on which led to many breakthrough discoveries in the scientific world. The cells were later named HeLa cells. No one in her family knew about this until years after her death, so they felt like she was just being used as an experiment from which they got nothing. When looking at the book as a whole, it is easy to see why so many people hold it in such high regards; however it appealed to me in a different way.