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       018                                                                                     HEALTH AND LABORATORY MAGAZINE
























                                THE FIRST SCIENTIST AND

                                ENTREPRENEUR, DR. CIHAN TAŞTAN, WHO

                                STORES DIGITAL DATA IN DNA IN TURKEY:

                                FUTURE OF GENE THERAPY AND CRISPR

                                GENE EDITING




       WE HAD A USEFUL INTERVIEW WITH DR. CIHAN TAŞTAN, ACIBADEM LABCELL CELL LABORATORY,
       MOLECULAR BIOLOGIST / R&D OFFICER. WE TALKED ABOUT THEIR PROJECTS THAT HELPED
       THEM BECOME PIONEERS IN TURKEY IN THE START OF GENETIC TREATMENTS.
       WE TOUCHED UPON MANY FIELDS FROM GENE THERAPIES TO CRISPR TECHNIQUE, FROM
       SYNTHETIC BIOLOGY TO DNA DATA STORAGE METHODS, FROM HIDNA TO LOCAL BIO-HACKERS.
       WE WOULD LIKE TO THANK DR. CIHAN TAŞTAN ON BEHALF OF OUR READERS INTERESTED IN THE
       SUBJECT, AND WISH YOU A PLEASANT READING.



       You are working as an R&D   in other genetic-based   should focus on specific   human cells with a maximum   I work especially on genetic
       Specialist at Acıbadem   diseases. We have now     problems, goals and objec-  of 1% efficiency in our first   engineering, gene therapies
       LabCell Cell Laboratory to   prepared our genetic   tives.  Although the funds   experiments, we continued   and synthetic biology. I
       develop gene therapies.   designs for diseases on our   allocated to the academy   to optimize without giving   believe that the fields I
       What do you do here?     list such as Adenoleukodys-  are limited, I believe that   up because we knew that   work in, which enable the
                                trophy, Duchenne Muscular   sufficient research funding   this technology would   production of value-added
       Acıbadem LabCell Labo-   Dystrophy, β-Talesemia and   has been provided to solve   revolutionize the medicine.   products in many fields I
       ratory continues its studies   Hemophilia. In the future, we   many of our problems.   When we showed within six   call bioindustry, are better
       especially in root cellular   aim to be the first in the local               months that we could delete   understood by our country
       therapies and cord blood   production of genetic and   Since 2012, researchers   any desired target gene with   day by day.  I carry out my
       banking under the leader-  cellular therapies for these   have started to perform   95% efficacy using lentiviral   studies in every field that
       ship of Prof. Dr. Ercüment   diseases.             genome modifications      systems, no one had yet   revolves around DNA, from
       Ovalı.  As Acıbadem Labcell                        with CRISPR technique by   managed to demonstrate   genetic treatments that will
       Laboratory, we have been a   What would you say about   producing synthetic and   effective genome modifi-  end our external depend-
       pioneer in Turkey in the start   being a scientist in Turkey?   specific DNA sequences   cation in human immune   ency in terms of drugs and
       of genetic treatments as   Do you find the studies   that are similar to CRISPR   system cells.  CRISPR tech-  ensure the improvement of
       well as cellular treatments.    conducted on science and   DNA sequences. You have   nology was a new turning   many diseases at once, to
       We performed the first   genetics in our country   actualized the project    point in my doctoral thesis.    the synthetic biology where
       clinical trial with genetically   sufficient?      of developing CRISPR      Two of our scientific articles,   we can store any size of
       modified cells in the history                      genome modification       which we carried out with the   information in DNA. In the
       of Turkish Medicine in ALL   I think in Turkey, the scien-  techniques in human   great influence of CRISPR   near future, when countries
       and NHL blood cancers in   tists are in search.  I also be-  immune system cells. What   technology during my PhD,   enter a billions of dollars in
       early 2019.  We have now   lieve there is a lack of goals   did you experience in this   were published in the journals   an economic race in these
       modified the cells we receive   and objectives. Being an   process?          Nature Mucosal Immunology   fields, we should try to pro-
       from our patients using   academician or a scientist is                      and Journal of Immunology.  duce as much local know-
       lentiviruses with our genetic   not just finding an answer to   In the first months of 2015,          how as we can so that our
       designs that can genetically   a scientific question. Seeing   I was in the middle of my   Biotechnology, which   country does not fall behind
       recognize ALL and NHL    the problems, turning them   doctorate study.  My counse-  has been in our lives for   in this race.
       cancer types under special   into questions and finding   lor Prof. Dr. Derya Unutmaz   almost half a century in
       laboratory conditions (BSL3   an answer and a solution to   (The Jackson Laborato-  the industrial sense, has   Recently, you have put
       virus and GMP laboratories).   them with scientific methods   ry-Genomic Medicine),   not only been a tool for   your signature under an
       We detected a significant   are among the tasks of sci-  who wanted an emergency   the production of some   important study, a first
       reduction in the cancer bur-  entists.  In other words, hav-  meeting one morning, asked   economically useful   in Turkey. After your
       den of our patients clinically   ing hundreds of universities   me to stop my thesis studies.   products in nature, but has   NHL patient, you have
       before the end of first two   should show us that there   She said that our new goal   passed into a ‘synthetic’   also transplanted the
       weeks.  While these studies   are thousands of scientists   is to apply CRISPR / Cas9   revolution used to design   genetically modified CAR-T
       are continuing, we started   who can find solutions to   genome modification tech-  new product combinations   immune cell that you
       our studies to use our ge-  our hundreds of problems,   nology in human immune   or processes that are   produced exclusively for
       netic design and lentivirus   invent products and let   system cells. Although we   not found in the nature.    your second patient (ALL).
       producing experiences in   people up.  For this reason,   managed to optimize the   What do you think about   What did you experience in
       clinical product standards   I believe that our scientists   genes we want to erase in   ‘Synthetic Biology’?  this process?
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