Full Answer Section

• Exploitation: I would be concerned that my mother’s cells were being exploited for commercial purposes. I would also be concerned about the potential for HeLa cells to be used for unethical research, such as human cloning or genetic engineering.

Research institutions can take a number of steps to protect and educate for the implications of Henrietta Lacks’ contribution to science. Here are a few suggestions:

• Obtain informed consent: Research institutions should obtain informed consent from all participants in research studies. This means that participants should be fully informed about the risks and benefits of the study before they agree to participate.
• Share benefits: Research institutions should share the benefits of research with participants and their families. This may include financial compensation, access to new treatments, or other benefits.
• Educate about HeLa cells: Research institutions should educate the public about HeLa cells and their importance to science. This will help to raise awareness of Henrietta Lacks’ legacy and the ethical implications of her contribution.

Henrietta Lacks’ legacy is complex and multifaceted. On the one hand, she is celebrated for her contribution to science. HeLa cells have been used to develop many important medical advances, including the polio vaccine and cancer treatments. On the other hand, Henrietta Lacks’ story is a reminder of the ethical challenges posed by medical research.

Here are some specific ways in which Henrietta Lacks’ legacy is being honored and preserved:

• The Henrietta Lacks Foundation: The Henrietta Lacks Foundation is a non-profit organization that provides support to Henrietta Lacks’ family and other families who have been affected by medical research. The foundation also works to raise awareness of Henrietta Lacks’ story and the ethical implications of medical research.
• The Lacks Family Biorepository: The Lacks Family Biorepository is a research repository that houses samples of Henrietta Lacks’ DNA and other genetic material. The biorepository is open to researchers who are working on projects that benefit the Lacks family or humanity as a whole.
• The Henrietta Lacks Legacy Act: The Henrietta Lacks Legacy Act is a proposed piece of legislation that would require research institutions to obtain informed consent from all participants in research studies and to share the benefits of research with participants and their families.

Henrietta Lacks’ legacy is a reminder of the power of science and the importance of ethical research practices. Her story has inspired a new generation of scientists and activists who are working to ensure that all people benefit from medical research.