Department/Affiliation: McKusick-Nathans Institute of Genetic Medicine
Johns Hopkins University School of Medicine
A few days ago I
found myself sitting next to a news reporter at a scientific meeting who
lamented that all this beautiful work done by scientists is never explained
properly to the public and how the gap between science and general society is
increasing. That got me thinking—are scientists becoming too insular? What
should we do to re-engage the public?
One of the recent events that highlighted this
was the report by a research group in China of editing human embryos using
CRISPR/Cas9 (Protein Cell. 2015
May;6(5):363-72.). Though the paper clearly mentioned that these double
fertilized embryos were naturally non-viable and the experiment showed many off
target effects and more detail studies were required, the general public got
the impression from the mainstream press that we were in the era of designer
babies. As scientists held nuanced debates in many scientific forums, none of these
were properly conveyed to the public, and the long-term benefits and
application of such techniques were not highlighted. Sadly, even the ethics
debate was not properly conducted, leaving behind a trail of unanswered
questions and misinformation creating a false image of crazy scientists
creating a Frankenstein.
Two initiatives
in 20th century America perfectly highlight the potential benefits
of engaging the public in the scientific journey. The first is the formation of
The National Foundation for Infantile Paralysis by president
Franklin D. Roosevelt, which was made popular by Eddie Cantor’s radio appeal to
the people to send dime(s) for the cause of polio research, thus renaming the
organization –The March of Dimes Birth Defects Foundation. This popular appeal
galvanized the general public by making them partners in the research progress.
The second was the joint effort by Sidney Farber and Mary
Lasker to raise awareness about cancer among the people and highlight the need
for a more concerted effort to find a cure doing better research and eventually
leading to the National Cancer Act, 1971, the positive effect of which is felt even
today by cancer researchers as well as by patients and families. This monumental
effort made the general public aware of the various nuances of research on
cancer and the difficulties associated with them, thus making science a little
less mysterious and the scientists a bit more human (for a more detailed
account read Siddhartha Mukherjee’s “The Emperor of All Maladies”).
Scientists will benefit in the long run from this
inclusiveness. As we engage the public and make them aware of our work, it will
lead to a change of perception and more popular support for the practice of
science. This, in turn, will lead to policy- and decision-makers allocating
more resources and allowing for better research to be conducted that will
justify the investment.
Sumantra Chatterjee is a postdoc at the Johns Hopkins University School of Medicine in Baltimore, Maryland, where his research focus is on understanding networks implicated in complex human disorders.
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