Henrietta Lacks Test Answers


  • In the laboratory, her cells turned out to have an extraordinary capacity to survive and reproduce; they were, in essence, immortal. The researcher shared them widely with other scientists, and they became a workhorse of biological research. Today,...
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  • But the story of Henrietta Lacks also illustrates the racial inequities that are embedded in the US research and health-care systems. Lacks was a Black woman. The hospital where her cells were collected was one of only a few that provided medical...
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  • Many people have also told him that they were able to conceive a child because of in vitro fertilization, which was developed with the help of HeLa cells. And they do so for people of all ethnicities. Policy review Over the past decade, scientists and the Lacks family have worked together to establish stronger rules to govern the use of these precious specimens. But there is still much work to be done. First is action on consent. NIH director Francis Collins has signalled that he wants the research community to consider changing the Common Rule, the set of policies that protect human participants in research funded by the US government 2. Most popular human cell in science gets sequenced Earlier efforts to make this change failed in , but now is the time to revisit the Common Rule, and to reconsider the question of consent. In the past, some researchers have warned that this would impose additional burdens.
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  • But a compromise must be found. The last time the US Department of Health and Human Services worked to revise the Common Rule, it proposed a series of other changes at the same time; perhaps one way forward is to tackle the question of consent for biospecimens on its own, and with thorough discussion involving not only scientists, but also the public. In the current climate of reckoning with racial injustice, some researchers who use HeLa cells have concluded that they should offer financial compensation. For example, a laboratory at the University of California, San Diego, and a UK-based biomedical company have announced donations to the Henrietta Lacks Foundation, which was established in by Rebecca Skloot, the author of a book about Lacks. Other institutions and researchers must examine whether — and how — their own work builds on past injustices. And they must consider how best to make amends. COVID, a disease that is disproportionately affecting Black people in a number of countries, offers an opportunity for those who wish to usher in a fairer era of research.
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  • To give back now, researchers should not only study why the disease is more prevalent and severe among Black people, but also help to implement solutions to close the gap. And, once a vaccine is available — possibly as a result of work with HeLa cells — researchers must work with marginalized communities to see that it reaches those who need it most. The past cannot be undone, but we must acknowledge the wrongs of previous generations, and those wrongs that persist today. Justice must be done, and the time to start is now. Nature , 7
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  • Answers to multiple choice questions for The Immortal Life of Henrietta Lacks that test students' recall and understanding of the work. This section contains 4, words approx. What did Henrietta Lacks tell her two cousin, Margaret and Sadie that they never told her husband? What did Henrietta Lacks' doctor tell her to go to Johns Hopkins? One of the top hospitals that treated black people and the syphilis sore tested negative. Ask and answer questions about the novel or view Study Guides, Literature Essays and more.
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  • The Question and Answer sections of our study guides are a great resource to ask questions, find answers, and discuss literature. How is the Great Migration explained in this novel? Why was it significant in Henrietta and Days life? Jack Ryan 4. Barbie as a weapon 5. Madame Alexander - 6. It's also the story of racial politics and medical ethics, and how both of those things have evolved or not in the years since Henrietta's death.
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  • Find the quotes you need to support your essay, or refresh your memory of the book by reading these key quotes. Their Research. Your Permission? Deborah Lacks holding an image of HeLa cells. Her book The Immortal Life Of Henrietta Lacks was incredibly well researched and spent 75 weeks on the Informed consent is the key when not under distress or duress or potentially tortured into complying. These cells launched a medical revolution and are still alive today. Her experience and that Though she died of cancer in , her immortal cells became the foundation Henrietta was not one to complain, but, according to the book The Immortal Life of Henrietta Lacks by Rebecca Skloot, she could no longer bear A black woman who grew up poor on a tobacco farm, she married her cousin The Immortal Tale of Henrietta Lacks has received considerable acclaim.
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  • It is all well-deserved. The book is an eye-opening window into a piece Lacks, Rebecca Skloot documents the histories of. Henrietta's hus-. It was the winner of the National Academies Communication Award for best creative work that helps the public understanding of topics in science, engineering or medicine. People wanted to know: did scientists And a few scientists decided to prove it. Skloot, Rebecca. Henrietta Lacks was a year-old black mother of five in Baltimore when she died of cervical cancer in Without her knowledge, doctors treating her at Johns Hopkins took tissue samples from her. The Lacks family felt for years that they had been mistreated by medical professionals and were taken advantage of because of their connection to HeLa.
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  • On what date did Henrietta Lacks first go to Johns Hopkins to have the knot in her womb examined? January 29, Who were Henrietta's cousins that she first told about the knot she felt in her womb, prior to her visit to the hospital? Sadie and Margaret. How old was Henrietta Lacks when she became pregnant with her fifth child? What was the birth name of Henrietta Lacks's fifth child? Joseph Lacks. When was Johns Hopkins Hospital founded? Who was the gynecologist that examined Henrietta Lacks when she first went to Johns Hopkins Hospital to have the knot in her womb seen? Howard Jones. What was Henrietta Lacks's name at birth? Loretta Pleasant. This section contains 4, words approx.
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  • Hindustan Times, New Delhi By hindustantimes. Scientists and frontline workers are being hailed for their selfless service, but one individual who awaits her due is Henrietta Lacks — a black tobacco farmer who died at 31 from an aggressive form of cancer. Who is Henrietta Lacks and why is she important? Henrietta Lacks was diagnosed with cervical cancer in at the age of just At the time, many hospitals in the US practised segregating black patients from white patients, which reduced her options for seeking treatment. She ended up at Johns Hopkins Hospital in Baltimore, Maryland, in a ward located down the hall from George Gey, a researcher who had been attempting to grow human cells in his lab for decades. Her doctor sent some of her cells to Gey without her consent, changing the course of medicine forever. Soon scientists all over the world started using her cell lines for furthering their research.
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  • The HeLa cells, however, spell out a different set of questions and possibilities. Once vaccination commences in full swing, a chance to correct a historical wrong will present itself.
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  • What does Skloot describe at the beginning of the Prologue? How does Skloot introduce Henrietta at the beginning of the story? What facts are provided by Skloot to give readers an idea of the scope of HeLa cell production? Where did Skloot first learn about Henrietta? How did Skloot become curious about Henrietta? What does Skloot decide she wants to do when she learns that Henrietta's family has been left out of the loop by the medical establishment?
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  • Which member of the Lacks family does Skloot most closely bond with? Why does Skloot find her beliefs and assumptions challenged while spending time with Deborah? What story does Skloot say that the book tells? Answers 1. A photo of Henrietta Lacks that she keeps on her wall 2. As the unidentified patient whose cancerous cells were taken and used to create HeLa cells, the first immortal cell line 3. There are trillions of Harriet's cells growing in laboratories all around the world, which are used for all kinds of scientific research. In a community college bio class 5. Her teacher doesn't have any details about Henrietta's life. Tell the family's story 7. Henrietta's daughter, Deborah 8. Deborah and Skloot are completely different in their thinking and experiences.
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  • Explain using examples from the book. Why did Dr. Gey give HeLa samples to his colleagues? Did he make any money off of the cells? Why or why not? Discuss how people were able to create lucrative businesses out of HeLa cells. Who was Southam and what did he do? How does this book relate to the Nuremberg codes? Discuss examples of unethical biomedical research provided in this book. Discuss the treatment of the mentally ill and developmentally disabled in s and 60s America. How does this affect the Lacks family? Responses must include a brief introduction, conclusion, and body paragraphs and use evidence and examples from the book to support your answers.
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  • How have HeLa cells impacted modern medicine? How are they still relevant today? How far has cell development come since HeLa cells were first introduced? As the book progressed, how did the relationship between Deborah and the author change? Was the initial tension merely a racial tension? Or were there other issues? Did the author have the same effect on the other Lacks children? Order now and Get a Discount! Share this entry.
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  • This is her journalistic technique for telling a story that largely has to do with complicated scientific advances—she never lets her readers forget about the human beings behind those advances, and the lives they led. At first, she believes that it has to do with having given birth to Deborah a few weeks earlier, or to the STIs that David Lacks has given her in the past by being unfaithful. However she refuses to get it checked.
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  • She is intuitive, but also very stubborn. Active Themes About a week later, the twenty-nine-year-old Henrietta is pregnant yet again with Joe, her fifth child. Sadie and Margaret believe that the pain had to do with the baby, but Henrietta disagrees. About four and a half months after Joe is born, Henrietta finds blood in her underwear. As the narrative goes forward, readers will better understand the reasons for the deep fear that Henrietta and her family have for the medical establishment, which fuels her reluctance to seek a diagnosis for the lump on her cervix. Howard Jones, an older Southern doctor, treats her. He reads her chart, finding many conditions that Henrietta has left untreated throughout the years. The chart also details that Henrietta has an epileptic daughter. Two months ago, after delivering Joe, Henrietta had significant blood in her urine, and the cells around her cervix seemed abnormal. Despite a doctor recommending further tests, Henrietta canceled her appointment.
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  • During this time, black women simply did not get the medical care that they needed—afact that will cost Henrietta her life. Jones about the pain and the blood, and adds that she has found a lump in her cervix. He examines her and finds the lump. Jones takes a sample and sends it to a lab for a diagnosis. At the same time, the narrative is concerned not just with the medical oddity of the tumor, but about the effect it will have on Henrietta, continuing the pattern of balancing scientific fact with personal narrative.
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  • Courtesy of the Lacks family smithsonianmag. In , a scientist at Johns Hopkins Hospital in Baltimore, Maryland, created the first immortal human cell line with a tissue sample taken from a young black woman with cervical cancer. Those cells, called HeLa cells, quickly became invaluable to medical research—though their donor remained a mystery for decades. In her new book, The Immortal Life of Henrietta Lacks, journalist Rebecca Skloot tracks down the story of the source of the amazing HeLa cells, Henrietta Lacks, and documents the cell line's impact on both modern medicine and the Lacks family.
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  • She was a black tobacco farmer from southern Virginia who got cervical cancer when she was A doctor at Johns Hopkins took a piece of her tumor without telling her and sent it down the hall to scientists there who had been trying to grow tissues in culture for decades without success. No one knows why, but her cells never died. Why are her cells so important? They were essential to developing the polio vaccine. They went up in the first space missions to see what would happen to cells in zero gravity. Many scientific landmarks since then have used her cells, including cloning, gene mapping and in vitro fertilization. There has been a lot of confusion over the years about the source of HeLa cells. When the cells were taken, they were given the code name HeLa, for the first two letters in Henrietta and Lacks. Today, anonymizing samples is a very important part of doing research on cells. Other pseudonyms, like Helen Larsen, eventually showed up, too. How did you first get interested in this story?
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  • I first learned about Henrietta in I was 16 and a student in a community college biology class. The moment I heard about her, I became obsessed: Did she have any kids? What do they think about part of their mother being alive all these years after she died? Years later, when I started being interested in writing, one of the first stories I imagined myself writing was hers. A HeLa cancer cell dividing. These cells are shown in green the cytoplasm is red and structures within the cytoplasm are blue. I knew she was desperate to learn about her mother. I went down to Clover, Virginia, where Henrietta was raised, and tracked down her cousins, then called Deborah and left these stories about Henrietta on her voice mail. Twenty-five years after Henrietta died, a scientist discovered that many cell cultures thought to be from other tissue types, including breast and prostate cells, were in fact HeLa cells.
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  • It turned out that HeLa cells could float on dust particles in the air and travel on unwashed hands and contaminate other cultures. It became an enormous controversy. And now we have to test your kids to see if they have cancer. How did they do that? Deborah never knew her mother; she was an infant when Henrietta died. She had always wanted to know who her mother was but no one ever talked about Henrietta. So when Deborah found out that this part of her mother was still alive she became desperate to understand what that meant: Did it hurt her mother when scientists injected her cells with viruses and toxins?
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  • Had scientists cloned her mother? And could those cells help scientists tell her about her mother, like what her favorite color was and if she liked to dance. HeLa cells were the first human biological materials ever bought and sold, which helped launch a multi-billion-dollar industry. One of her sons was homeless and living on the streets of Baltimore. So the family launched a campaign to get some of what they felt they were owed financially.
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  • It consumed their lives in that way. These HeLa cells were stained with special dyes that highlight specific parts of each cell. The DNA in the nucleus is yellow, the actin filaments are light blue and the mitochondria—the cell's power generators—are pink. Courtesy of Random House, Inc. Skloot first learned about Henrietta in from a community college biology teacher. What are the lessons from this book? For scientists, one of the lessons is that there are human beings behind every biological sample used in the laboratory. So much of science today revolves around using human biological tissue of some kind. And for the rest of us? The story of HeLa cells and what happened with Henrietta has often been held up as an example of a racist white scientist doing something malicious to a black woman.
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  • The real story is much more subtle and complicated. What is very true about science is that there are human beings behind it and sometimes even with the best of intentions things go wrong. So much of medicine today depends on tissue culture. And the need for these cells is going to get greater, not less. Like this article? She is a contributing writer in science for Smithsonian.
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  • On February 1,under the cover of a solitary tree, David Lacks stared through the window of his parked car, watching the rain fall. He and his five children, three still in diapers, sat outside Hopkins Hospital, waiting for Henrietta. A few days earlier, she had found blood spotting her underwear. Now, Howard Jones, a Hopkins physician, found a smooth eggplant-hued tumor glistening under the light on Henrietta's cervix. He touched its surface, shocked by its supple texture, and Henrietta bled. Jones carefully cut a section of her quarter-sized tumor, sent it to the lab for a diagnosis, and sent Henrietta home with her henrietta lacks test answers. Then came the news: the tumor was malignant.
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  • Henrietta returned to Hopkins eight days later. While David and the children waited under the tree, physicians covered her cervix with radium in an attempt to kill the cancer. But before applying the first treatment, a young resident took one more sample. This one went to George Gey, head of tissue culture research at Hopkins. He and his wife, Margaret, had been searching for a tool for the study of cancer: a line of human cells that would live indefinitely outside the body.
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  • If they succeeded, they could observe and test human cells in ways they could never do in humans. Eventually, they hemrietta discover the cure for cancer. They were sure of it. After two decades of failure in their laboratory attempts, the Geys turned their attention to cervical cells, at the henriettta of Richard TeLinde, then Hopkins lafks of Gynecology. Henrietta lacks test answers wanted cervical cells for his own research; the Geys wanted any cancer cells they could get. The day George Gey got his hands on Henrietta Lacks's cells, everything changed. For the Geys, for medicine, and eventually for the Lackses.
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  • The day George Gey got his hands on Lacks's cells, everything changed. They latched to the sides of test tubes, consumed the medium around them, and within days, the thin film of cells grew thicker and thicker. But Henrietta's tumor cells took over her body as quickly as they'd taken over test tubes. Within months, tumors appeared on almost every organ, and Henrietta moaned from her bed for the Lord to help her. The day she died, October 4,George Gey appeared on national television with a vial of Henrietta's cells. He called them HeLa cells, held them up answerd the camera, and said, "It is possible that, from a fundamental study such as this, we will be able to learn a way by which cancer can be completely wiped out.
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  • And her family knew nothing of any cells. As a train carrying Henrietta's casket rolled back toward Virginia, her cells shocked Gey with their strength. The local undertaker met Henrietta's body at the station where, less than a decade annswers, she had boarded her train to Baltimore. He buried her in an unmarked grave across the street from her family's tobacco field, behind the house where her mother was born. But in the Lacks family cemetery, where cattle roam freely when the season's right, folks today don't know much about HeLa. They don't know that soon after Henrietta's death inGey and his colleagues used her cells to grow the polio virus that was ravaging children throughout the world.
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