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    • The Fascinating Story of Henrietta Lacks and Her Immortal CellsHenrietta Lacks' cancer cells, taken without consent, have been used in countless scientific discoveries, highlighting the importance of informed consent and ethical considerations in medical research.

      This episode of "This Podcast Will Kill You" explores the fascinating story of Henrietta Lacks and her immortal cells. Henrietta Lacks was a woman whose cancer cells were taken without her consent and have since been used in numerous scientific research and discoveries. The hosts, Erin Welsh and Erin Almond Updike, discuss various aspects of this topic, including tissue culture, informed consent, and who Henrietta Lacks was as a person. They begin the episode with a discussion about ambrosia, a drink inspired by the theme of immortality. The hosts also mention various resources for listeners to access, such as their website, social media channels, Goodreads list, bookshop.org link, and merchandise by independent artists. Overall, this episode offers a unique and thought-provoking exploration of an important chapter in medical history.

    • The Beginning of Cell Culture: Henrietta Lacks' HeLa CellsHenrietta Lacks' HeLa cells marked the beginning of cell culture technology, providing a consistent and renewable source of cells for scientific research, leading to numerous breakthroughs and advancements in our understanding of biology and medicine.

      Cell culture technology has revolutionized various fields of biology and medicine, allowing for the study of fundamental cellular mechanisms, the development of vaccines and therapeutics, and the production of essential biopharmaceuticals. The significance of cell culture technology can be traced back to the discovery of Henrietta Lacks' HeLa cells, which were the first human cells to be grown indefinitely in a lab. Before HeLa cells, scientists struggled to keep mammalian and human cells alive for extended periods. Henrietta Lacks' cervical cancer cells, which were taken without her consent, did not die but continued to grow and replicate, marking the beginning of cell lines. Cell lines are essential for scientific research as they provide a consistent and renewable source of cells, enabling researchers to study various biological processes and test the effects of drugs, viruses, and other agents on cells over extended periods. The impact of HeLa cells and subsequent cell lines on scientific research is immeasurable, leading to numerous breakthroughs and advancements in our understanding of biology and medicine.

    • Cells' growth and division mechanisms and the role of telomeres and telomerase in cancerCancer cells can bypass normal growth and division limitations through telomerase activation, leading to indefinite division and rapid growth. Telomeres and telomerase also impact aging process.

      Cells have various mechanisms to ensure appropriate growth and division, including proteins that regulate the cell cycle and telomeres that act as protective caps on chromosomes. However, some cells, like cancer cells, can bypass these limitations through the activation of telomerase, an enzyme that extends telomeres and allows for indefinite cell division. This is a key factor in cancer's ability to persist and grow rapidly. Furthermore, telomeres and telomerase are also linked to the aging process, as faster cell turnover due to stress or inflammation can lead to shorter telomeres and faster aging. However, it's important to note that cancer cells typically have multiple mutations, including those in telomerase and other cell cycle regulators, making the development of a cancer cell a complex process.

    • Immortalized cell lines vs stem cellsImmortalized cell lines, like HeLa, are created from differentiated cells and can divide indefinitely. They're essential for research but distinct from stem cells, which are undifferentiated and can become any cell type.

      Cell lines, like HeLa, are created by making cells immortal through various means such as introducing viral vectors or activating telomerase. These immortalized cells come from differentiated tissues and can divide indefinitely while retaining the potential to become various cell types. This is different from stem cells, which are undifferentiated cells that can become any cell type and are found both in embryos and in adults. While both immortalized cell lines and stem cells are essential for scientific research, they have distinct differences. It's important to note that while the vast majority of cervical cancers are caused by HPV, there are still some cases that are not associated with HPV. And finally, the current status of cell culture includes a wide range of cell lines from various animals and tissues that serve specific purposes.

    • Respecting the humanity behind the cellsRemember that each data point in science represents an individual with a rich history and life, contributing to better scientific practices and human compassion

      While stem cells, such as epidermal and hematopoietic, have the unique ability to divide and differentiate into various cell types, it's important to remember that they originate from human beings with complex histories and lives beyond their cellular functions. For instance, Henrietta Lacks, a black woman who died of cervical cancer in 1951 at the age of 31, is known for being the source of the HeLa cell line, which has been instrumental in scientific research. However, she was more than just a cell donor; she was a mother, a daughter, a wife, and a friend. The tendency in science and medicine to focus on measurable data can sometimes lead to a loss of sight of the humanity behind the numbers. It's crucial to remember that each data point represents an individual with a rich history and life, which likely contributes to better scientific practices and overall human compassion.

    • The Life of Henrietta Lacks: A Simple Woman with an Extraordinary ImpactHenrietta Lacks, a simple woman from Virginia, unknowingly contributed to medical advancements through the first immortal human cell line, despite facing personal struggles and lack of consent.

      Henrietta Lacks, a real person born in 1920, lived a simple life in Virginia before moving to Baltimore for industrial jobs during World War 2. She was known for being an amazing cook and spending time with her family. However, she faced tough times, including the death of her daughter Elsie in a mental hospital. In 1951, Henrietta visited Johns Hopkins Hospital for a knot on her womb, which was later discovered to be cancer. Her cells, taken without her consent, became the first immortal human cell line, leading to significant medical advancements. This episode highlights the importance of acknowledging the real people behind scientific discoveries and the ethical implications of medical research.

    • Discovery of the First Immortal Human Cell Line from Henrietta LacksThe discovery of Henrietta Lacks' immortal HeLa cell line revolutionized medical research, but its acquisition without her consent sparked ethical debates.

      Henrietta Lacks' cervical tumor, which was removed in 1951, led to the discovery of the first immortal human cell line, named HeLa. This discovery revolutionized medical research, but at the time, it was standard practice for doctors to take tissue samples without the patient's knowledge or consent. The tissue was given to researchers, like George and Margaret Guy, who had been working for decades to find an immortal human cell line. Despite their previous failures, they believed that HeLa could be the answer to their quest. They extracted tissue samples from Henrietta's tumor and normal tissue, which were then sent to a lab for culturing. The lab employee, Mary Kubacek, processed the tissue and labeled the culture tubes with Henrietta's name. Initially, she didn't expect much from the samples, but HeLa cells proved to be unique and immortal, leading to significant medical advancements. However, the ownership and ethical implications of using Henrietta's cells without her consent became a topic of controversy in later years.

    • The Discovery of Henrietta Lacks' Immortal CellsHenrietta Lacks' unknowingly donated cells led to countless medical advancements, but her family was unaware and lacked consent.

      The discovery of Henrietta Lacks' immortal HeLa cells revolutionized medical research, leading to countless advancements, but her contribution and consent were overlooked. Dr. Richard Tilland, a gynecologist, believed that cervical cancer cells were dangerous and formed a deal with George Gey to provide tissue for culturing. Henrietta's tissue, taken without her knowledge or consent, produced the first immortal human cell line. Despite the widespread use of HeLa cells, Henrietta and her family remained unaware until her death in 1951. Her autopsy was performed without explicit consent for further sample collection. This story highlights the ethical dilemmas surrounding medical research and the importance of informed consent.

    • Henrietta Lacks and the Ethical Dilemmas of Medical ResearchThe story of Henrietta Lacks and her HeLa cells highlights the importance of informed consent in medical research and the far-reaching implications of scientific discoveries, while also raising ethical questions about the use of cells taken without consent in the past.

      The story of Henrietta Lacks and her HeLa cells highlights the complex ethical issues surrounding consent in medical research, which was less strictly regulated in the past than it is today. Henrietta's cells, taken without her knowledge or consent during her autopsy, went on to revolutionize scientific research in various fields, including virology, genetics, and cell biology. The demand for HeLa cells was immense due to their ease of cultivation and versatility, leading to their use in research on polio vaccines, chromosome discovery, radiation effects, and many other topics. The ethical dilemmas surrounding Henrietta's story continue to resonate, as her cells are still being used today and her family only learned about their use decades later. This episode underscores the importance of informed consent in medical research and the far-reaching implications of scientific discoveries.

    • The Unauthorized Use of Henrietta Lacks' Cells in Scientific ResearchDespite using Henrietta Lacks' cells without her consent, they led to significant scientific advancements. However, ethical concerns and confusion arose when her family discovered the truth, emphasizing the importance of informed consent and patient confidentiality.

      The use of Henrietta Lacks' cells, taken without her consent, led to significant scientific advancements but also caused ethical concerns and confusion for her family. For 15 years, researchers used HeLa cells in various studies, but in 1966, it was discovered that many other cell lines were contaminated with HeLa cells, leading to wasted research funds and time. Although Henrietta's real name and connection to the cells began to be known among researchers, her family remained unaware until 1973 when a chance encounter revealed the truth. The incident highlights the importance of informed consent and patient confidentiality, which were not as well-established during that time. It also underscores the ethical implications of using human cells for research without the knowledge or consent of the donor and their family.

    • Henrietta Lacks and the Ethical Dilemma of Her Immortal HeLa CellsThe story of Henrietta Lacks highlights the importance of informed consent and transparency in scientific research involving human subjects, and the potential consequences of disregarding these ethical guidelines.

      The story of Henrietta Lacks and her immortal HeLa cells raises important ethical questions about informed consent, patient privacy, and the ownership of human cells in scientific research. Without her knowledge or consent, Henrietta's cells were taken after her death and used for research that led to numerous medical advancements. Over the decades, her family was left in the dark about the use of her cells and the resulting scientific discoveries. The lack of informed consent and transparency led to a long-lasting controversy that brought attention to the need for clear ethical guidelines in scientific research involving human subjects. Today, Henrietta's legacy extends beyond her scientific contributions, with efforts to acknowledge her and her family's role in medical history and to provide support and resources to individuals and families affected by similar situations.

    • HeLa cells revolutionized biomedical researchHeLa cells, obtained without consent in 1951, led to 110,000 research articles, 3 Nobel Prizes, and advancements in microscopy, gene therapy, cancer treatments, and organ growth. Ethical implications include lack of informed consent and family privacy.

      HeLa cells, derived from Henrietta Lacks without her consent in 1951, have revolutionized biomedical research. With over 110,000 research articles published using these cells, they have contributed to three Nobel Prizes, advancements in microscopy, gene therapy, cancer treatments, and even potential for growing human organs. However, the ethical implications of this discovery are significant. While HeLa cells have led to groundbreaking scientific achievements, they were obtained without informed consent, and her identity was revealed without her family's knowledge. Although there are regulations in place, such as the Common Rule, which allows for the use of biospecimens without informed consent if they are deidentified, the system is not foolproof. It's crucial to recognize the ethical complexities that arise from such discoveries and strive for more robust protections for human subjects in research.

    • The Use of Henrietta Lacks' HeLa Cells Raises Ethical ConcernsDespite new regulations, ethical concerns persist regarding the use of Henrietta Lacks' HeLa cells for genomic analysis due to advancements in technology outpacing ethics and laws.

      The use of HeLa cells, which were taken from Henrietta Lacks without her consent, raises ethical concerns, especially in light of advancements in technology that allow for genetic analysis and comparison across databases. Although some new regulations require informed consent for genomic analysis, the issue is outdated as technology moves faster than ethics and laws. However, there are signs of progress, such as donations to the Henrietta Lacks Foundation by research institutions and the NIH, and more conversations about reparations. The episode aims to raise awareness about this issue and the podcast, This Podcast Will Heal You, made a donation to the foundation as well. The sources for this episode are primarily "The Immortal Life of Henrietta Lacks" by Rebecca Skloot and a few articles.

    Recent Episodes from This Podcast Will Kill You

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    Ep 143 IVF, Part 1: Infertility
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    Special Episode: Dr. Noah Whiteman & Most Delicious Poison

    Special Episode: Dr. Noah Whiteman & Most Delicious Poison
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    Ep 142 Leeches: It’s more powerful than magic, it’s nature

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    Special Episode: Dr. Paul Offit & Tell Me When It’s Over

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    Ep 141 Maggots: Such noble work

    Ep 141 Maggots: Such noble work
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    Ep 139 Supplements: “This statement has not been evaluated by the FDA”

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    Special Episode: Dr. Deirdre Cooper Owens & Medical Bondage

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    Related Episodes

    SYSK Selects: How HeLa Cells Work

    SYSK Selects: How HeLa Cells Work

    In this week's SYSK Select episode, after she was diagnosed with the cervical cancer that shortly killed her, a tissue sample was taken from Henrietta Lacks in 1951 without her knowledge. Those cells would go on to become the first immortal line of human cells, something of enormous benefit to science and humanity as a whole. But while the line, called HeLa cells, became a multi-billion-dollar industry, her family languished without health care insurance. Learn about this complex case of private rights and scientific advancement in this episode.

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    Inflammation, Heart Disease, and the Environment: A Deep Dive with Douglas Mulhall

    Inflammation, Heart Disease, and the Environment: A Deep Dive with Douglas Mulhall

     

    In this episode of the "No Sitting on the Sideline Dad" podcast, we welcome Douglas Mulhall, a seasoned expert in the field of Environmental Health. With over 30 years of experience, Mulhall shares his unique insights into how our environment impacts our health and how our health, in turn, impacts the environment.

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    DOUGLAS MULHALL BOOKS BOOKS

     

    Website : www.natureoflongevity.com

     

    Episode 22: October 2022

    Episode 22: October 2022

    For this month’s episode, JHLT The Podcast explores two impactful studies from the October issue of The Journal of Heart and Lung Transplantation. The episode is hosted by Daniel R. Goldstein, MD, Editor-in-Chief of JHLT, who is joined by the JHLT Digital Media Editors. Listen now to hear study authors discuss their work, their studies, and next steps for their research.

    Michael Harhay headshotEdward Cantu headshotFirst, the editors speak with first author Michael Harhay, PhD (pictured left) and senior author Edward Cantu, MD (pictured right), about their study from the University of Pennsylvania entitled “Epidemiology, risk factors and outcomes of lung retransplantation: an analysis of the ISHLT Transplant Registry.” Dr. Goldstein and Erika Lease, MD, interview Drs. Harhay and Cantu about the study.

    The objective of the study was to leverage the ISHLT Thoracic Transplant registry using an updated cohort of patients that underwent lung retransplantation to obtain an updated summary of the epidemiology of lung retransplantation; to examine the importance of the time between primary transplantation and retransplantation on outcomes after retransplantation; and to identify risk factors of mortality following lung retransplantation.

    Anne Dipchand headshotNext, we hear from Anne Dipchand, MD (pictured), Professor of Pediatrics and Pediatric Cardiologist at the Hospital for Sick Children in Toronto, Canada, who is senior author on the study, “Eplet matching in pediatric heart transplantation: The SickKids experience.” Dr. Goldstein and David Schibilsky, MD, discuss the study with Dr. Dipchand.

    This single-center retrospective study measured allograft survival in 77 patients while performing HLA typing, antigen mismatch, and eplet mismatch analysis, with the goal of comparing the molecular level HLA matching with antigen level HL matching in post-heart transplant outcomes in children.

    Follow along in the October issue at www.jhltonline.org/current, or, if you’re an ISHLT member, log in at ishlt.org/journal-of-heart-lung-transplantation.  Don’t already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.

    Block the sun, save the earth?

    Block the sun, save the earth?
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