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“A SCANNER FOR HEREDITARY DEFECTS NEW

POSSIBILITIES IN GENETIC DAMAGE RECOGNITION

 FOR IMPROVEMENT CANCER TREATMENT” AND

“DISCOVERY OF NEW CLASS OF DAMAGE-PRONE

  DNA REGIONS COULD LEAD BETTER CANCER

              TREATMENTS” .
                      


         MOLECULAR BIOLOGY

        EMMANUEL SÁNCHEZ DÍAZ
     SECOND YEAR MEDICAL STUDENT
              MEDELLÍN
                2013
INTRODUCTION.
DNA is very susceptible to
damages because of the
permanent       exposure      to
several mutagenic factors. In
addition, DNA has some
fragile sites which makes it
more vulnerable to damage
especially in early stages of
the division cell cycle .
The recognition of a new
protein in charge of repairing
DNA damages (first new), and
the locations where DNA is
fragile (Second new) are
advances that provides new
tools     for     the     cancer
treatment.
A SCANNER FOR HEREDITARY DEFECTS: NEW
POSSIBILITIES IN GENETIC DAMAGE RECOGNITION
FOR      IMPROVING     CANCER    TREATMENT.
 
    Our genetic material is
    permanently     under     the
    effects of    several factors
    which may cause damages in
    the sequence that usually are
    repaired immediately by
    molecular control systems
    as p53 protein.
A SCANNER FOR HEREDITARY DEFECTS: NEW
POSSIBILITIES IN GENETIC DAMAGE RECOGNITION
FOR      IMPROVING     CANCER    TREATMENT.
 




                          Scientists discovered a
                          specially function of XPD
                          protein in the recognition
                          of these specific damaged
                          locations in the sequences
                          facilitating it´s eventually
                          reparation.
A SCANNER FOR HEREDITARY DEFECTS: NEW
POSSIBILITIES IN GENETIC DAMAGE RECOGNITION
FOR      IMPROVING     CANCER    TREATMENT.
 

     The XPD protein glides among the bases in
     search of damages in the sequence ,
     scientists describe it as a scanner. When the
     protein recognizes a damaged site, it stops
     and marks the location for its posterior
     reparation.
     The protein is also involved in processes as
     the cell cycle, genic expression, and others.
A SCANNER FOR HEREDITARY DEFECTS: NEW
POSSIBILITIES IN GENETIC DAMAGE RECOGNITION
FOR      IMPROVING     CANCER    TREATMENT.
 


While repairing DNA, XPD
protein    protects     the
tissues    health     from
damages in the genetic
material, but it also
diminishes the activity of
some     chemotherapeutic
drugs.
OP NION.
DISCOVERY OF NEW CLASS OF DAMAGE –
PRONE DNA REGIONS COULD LEAD BETTER
CANCER TRETMENTS.
                   Cancer could comes from a
                   damage in a specific locations
                   in    DNA     sequence,    these
                   sequences are thought to be
                   more vulnerable to damage.
                   Scientists     discovered    the
                   relationship between particular
                   fragile DNA sites and an specific
                   blood cancer called cell B
                   lymphoma.
DISCOVERY OF NEW CLASS OF DAMAGE –
PRONE DNA REGIONS COULD LEAD BETTER
CANCER TRETMENTS.


 The DNA damage could take
 place in different stages of the
 cell cycle, but it’s more
 common to occur during the
 early phases of the replication,
 before division. There are
 locations in the DNA sequence
 that are more vulnerable to
 DNA damages as         the very
 repetitive sequences where the
 DNA could break easily.
DISCOVERY OF NEW CLASS OF DAMAGE –
PRONE DNA REGIONS COULD LEAD BETTER
CANCER TRETMENTS.

                        Lymphocytes are cells with a high
                        division rate, that’s the reason why
                        they are more vulnerable suffering
                        damages during replication, in
                        addition during the non replicative
                        stage of the cell cycle, this cells
                        are very vulnerable to breaking in
                        the strand by the enzyme AID who
                        causes collateral damages in the
                        genome.



         The AID have no activity in several
         mutations associated in cell B
         lymphoma.
DISCOVERY OF NEW CLASS OF DAMAGE –
PRONE DNA REGIONS COULD LEAD BETTER
CANCER TRETMENTS.

   The scientists discovered a new kind of fragile sites called
   early replicating fragile sites (ERFSs) , the DNA damage at
   ERFSs occurs during early stages of replication. These sites
   have a high relationship with cell B lymphoma.
OP NION.
MEDICAL UTILITY.



   Cancer is a condition that concerns to all
   the    medical     sciences   since    it’s
   discovering.
   This disease has a particular etiology
   located in DNA sequence which is
   constantly attached by several factors
   that could affect the genome stability.
   In addition DNA has different vulnerable
   sites.
MEDICAL UTILITY.


        Advances allow us to recognize
        vulnerable locations of DNA and
        proteins involved in DNA damage
        reparation, this could lead us to
        improve the treatments against
        cancer and furthermore to
        manipulate the DNA sequence to
        make it “invincible”
MEDICAL UTILITY.


         The actual cancer treatments
         have a lot of secondary effects,
         diminishing the patients life
         quality, if we as scientists could
         intervene directly in the DNA
         sequence, we could eventually
         delete      the    uncomfortable
         therapy's and get better results
         in the battle against cancer
MEDICAL UTILITY.



         If we have the mechanisms to
        recognize the exact locations
        where DNA is damaged and mark
        this place, we could make
        quicker processes and improve
        the economical performance,
        reducing costs and improving the
        treatments.
THANKS!!!

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Folding molecular biology

  • 1. “A SCANNER FOR HEREDITARY DEFECTS NEW POSSIBILITIES IN GENETIC DAMAGE RECOGNITION FOR IMPROVEMENT CANCER TREATMENT” AND “DISCOVERY OF NEW CLASS OF DAMAGE-PRONE DNA REGIONS COULD LEAD BETTER CANCER TREATMENTS” .   MOLECULAR BIOLOGY EMMANUEL SÁNCHEZ DÍAZ SECOND YEAR MEDICAL STUDENT MEDELLÍN 2013
  • 2.
  • 3.
  • 4. INTRODUCTION. DNA is very susceptible to damages because of the permanent exposure to several mutagenic factors. In addition, DNA has some fragile sites which makes it more vulnerable to damage especially in early stages of the division cell cycle . The recognition of a new protein in charge of repairing DNA damages (first new), and the locations where DNA is fragile (Second new) are advances that provides new tools for the cancer treatment.
  • 5. A SCANNER FOR HEREDITARY DEFECTS: NEW POSSIBILITIES IN GENETIC DAMAGE RECOGNITION FOR IMPROVING CANCER TREATMENT.   Our genetic material is permanently under the effects of several factors which may cause damages in the sequence that usually are repaired immediately by molecular control systems as p53 protein.
  • 6. A SCANNER FOR HEREDITARY DEFECTS: NEW POSSIBILITIES IN GENETIC DAMAGE RECOGNITION FOR IMPROVING CANCER TREATMENT.   Scientists discovered a specially function of XPD protein in the recognition of these specific damaged locations in the sequences facilitating it´s eventually reparation.
  • 7. A SCANNER FOR HEREDITARY DEFECTS: NEW POSSIBILITIES IN GENETIC DAMAGE RECOGNITION FOR IMPROVING CANCER TREATMENT.   The XPD protein glides among the bases in search of damages in the sequence , scientists describe it as a scanner. When the protein recognizes a damaged site, it stops and marks the location for its posterior reparation. The protein is also involved in processes as the cell cycle, genic expression, and others.
  • 8. A SCANNER FOR HEREDITARY DEFECTS: NEW POSSIBILITIES IN GENETIC DAMAGE RECOGNITION FOR IMPROVING CANCER TREATMENT.   While repairing DNA, XPD protein protects the tissues health from damages in the genetic material, but it also diminishes the activity of some chemotherapeutic drugs.
  • 10. DISCOVERY OF NEW CLASS OF DAMAGE – PRONE DNA REGIONS COULD LEAD BETTER CANCER TRETMENTS. Cancer could comes from a damage in a specific locations in DNA sequence, these sequences are thought to be more vulnerable to damage. Scientists discovered the relationship between particular fragile DNA sites and an specific blood cancer called cell B lymphoma.
  • 11. DISCOVERY OF NEW CLASS OF DAMAGE – PRONE DNA REGIONS COULD LEAD BETTER CANCER TRETMENTS. The DNA damage could take place in different stages of the cell cycle, but it’s more common to occur during the early phases of the replication, before division. There are locations in the DNA sequence that are more vulnerable to DNA damages as the very repetitive sequences where the DNA could break easily.
  • 12. DISCOVERY OF NEW CLASS OF DAMAGE – PRONE DNA REGIONS COULD LEAD BETTER CANCER TRETMENTS. Lymphocytes are cells with a high division rate, that’s the reason why they are more vulnerable suffering damages during replication, in addition during the non replicative stage of the cell cycle, this cells are very vulnerable to breaking in the strand by the enzyme AID who causes collateral damages in the genome. The AID have no activity in several mutations associated in cell B lymphoma.
  • 13. DISCOVERY OF NEW CLASS OF DAMAGE – PRONE DNA REGIONS COULD LEAD BETTER CANCER TRETMENTS. The scientists discovered a new kind of fragile sites called early replicating fragile sites (ERFSs) , the DNA damage at ERFSs occurs during early stages of replication. These sites have a high relationship with cell B lymphoma.
  • 15. MEDICAL UTILITY. Cancer is a condition that concerns to all the medical sciences since it’s discovering. This disease has a particular etiology located in DNA sequence which is constantly attached by several factors that could affect the genome stability. In addition DNA has different vulnerable sites.
  • 16. MEDICAL UTILITY. Advances allow us to recognize vulnerable locations of DNA and proteins involved in DNA damage reparation, this could lead us to improve the treatments against cancer and furthermore to manipulate the DNA sequence to make it “invincible”
  • 17. MEDICAL UTILITY. The actual cancer treatments have a lot of secondary effects, diminishing the patients life quality, if we as scientists could intervene directly in the DNA sequence, we could eventually delete the uncomfortable therapy's and get better results in the battle against cancer
  • 18. MEDICAL UTILITY. If we have the mechanisms to recognize the exact locations where DNA is damaged and mark this place, we could make quicker processes and improve the economical performance, reducing costs and improving the treatments.
  • 19.