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DTSTAMP:20250204T101214Z
SUMMARY:Life Sciences Seminar: Bad Blood (feat. organ-on-chip):
 Recreating the bone marrow in the lab to study acute myeloid leukemia
DTSTART:20250303T180000Z
DTEND:20250303T185000Z
LOCATION:Thomas Gosnell Hall: A300
DESCRIPTION:<p class="default-image-margins"><span
 style="font-size:11pt"><span
 style="font-family:Calibri,sans-serif"><b><span
 style="font-family:&quot;Arial&quot;,sans-serif">Life Science
 Seminar</span></b></span></span><br>
 <span style="font-size:11pt"><span
 style="font-family:Calibri,sans-serif"><b><span
 style="font-size:16.0pt"><span
 style="font-family:&quot;Arial&quot;,sans-serif">Bad Blood (feat.
 organ-on-chip): Recreating the bone marrow in the lab to study acute
 myeloid leukemia</span></span></b></span></span></p>
 <p class="default-image-margins"><span style="font-size:11pt"><span
 style="font-family:Calibri,sans-serif"><b><span
 style="font-family:&quot;Arial&quot;,sans-serif"><span
 style="color:#ed7d31">Azmeer Sharipol, (RIT Biotechnology
 ’17)</span></span></b></span></span><br>
 <span style="font-size:11pt"><span
 style="font-family:Calibri,sans-serif"><span
 style="font-family:&quot;Arial&quot;,sans-serif">Ph.D. Candidate and NCI
 F99 Fellow, Biomedical Engineering</span></span></span><br>
 <span style="font-size:11pt"><span
 style="font-family:Calibri,sans-serif"><span
 style="font-family:&quot;Arial&quot;,sans-serif">University of Rochester
 Medical Center&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <b><span
 style="color:#ed7d31"></span></b></span></span></span><br>
 <span style="font-size:11pt"><span
 style="font-family:Calibri,sans-serif"><i><span
 style="font-family:&quot;Arial&quot;,sans-serif"><br>
 Abstract</span></i><span
 style="font-family:&quot;Arial&quot;,sans-serif">: <span
 style="background:white"><span style="color:black">Acute myeloid leukemia
 (AML) is an aggressive blood cancer that starts in the bone marrow.
 Current therapies for AML result in a 5-year survival rate of ~30%,
 highlighting the need for safer and more effective therapies. During AML,
 leukemia cells over-accumulate in the bone marrow and change the function
 of the surrounding cells to create a favorable environment for leukemia
 cell survival. The dysregulation of the bone marrow causes loss of normal
 hematopoiesis and is associated with the mortality and morbidity of AML.
 Our research goal is to develop a clinically relevant 3D model of the
 leukemic bone marrow microenvironment that can recapitulate the
 phenotypes of AML. We utilize a combination of organ-on-chip,
 microfluidics, and hydrogel technologies to successfully replicate the
 bone marrow that can maintain blood stem cell function and mimic the
 dysregulation due to leukemia
 cells.</span></span></span></span></span></p>
 <p class="default-image-margins"><i style><span style="font-family:
 Arial, sans-serif; font-size: 11pt;">Intended Audience:</span> </i><span
 style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span
 style="font-family:&quot;Arial&quot;,sans-serif">All are
 Welcome!</span></span></span></p>
 <p class="default-image-margins"><span style="font-size:11pt"><span
 style="font-family:Calibri,sans-serif"><span
 style="font-family:&quot;Arial&quot;,sans-serif">To request an
 interpreter, please visit <a href="https://myaccess.rit.edu/myAccess5/"
 style="color:#0563c1;
 text-decoration:underline">myaccess.rit.edu</a></span></span></span></p>
 <pre>
 <span style="font-size:11pt"><span
 style="font-family:Calibri,sans-serif"></span></span></pre>
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