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Surgery with molecular fluorescence imaging using activatable cell-penetrating peptides decreases residual cancer and improves survival

Identifieur interne : 001444 ( Ncbi/Merge ); précédent : 001443; suivant : 001445

Surgery with molecular fluorescence imaging using activatable cell-penetrating peptides decreases residual cancer and improves survival

Auteurs : Quyen T. Nguyen ; Emilia S. Olson ; Todd A. Aguilera ; Tao Jiang [États-Unis] ; Miriam Scadeng ; Lesley G. Ellies ; Roger Y. Tsien [États-Unis]

Source :

RBID : PMC:2840114

Abstract

The completeness of tumor removal during surgery is dependent on the surgeon’s ability to differentiate tumor from normal tissue using subjective criteria that are not easily quantifiable. A way to objectively assess tumor margins during surgery in patients would be of great value. We have developed a method to visualize tumors during surgery using activatable cell-penetrating peptides (ACPPs), in which the fluorescently labeled, polycationic cell-penetrating peptide (CPP) is coupled via a cleavable linker to a neutralizing peptide. Upon exposure to proteases characteristic of tumor tissue, the linker is cleaved, dissociating the inhibitory peptide and allowing the CPP to bind to and enter tumor cells. In mice, xenografts stably transfected with green fluorescent protein show colocalization with the Cy5-labeled ACPPs. In the same mouse models, Cy5-labeled free ACPPs and ACPPs conjugated to dendrimers (ACPPDs) delineate the margin between tumor and adjacent tissue, resulting in improved precision of tumor resection. Surgery guided by ACPPD resulted in fewer residual cancer cells left in the animal after surgery as measured by Alu PCR. A single injection of ACPPD dually labeled with Cy5 and gadolinium chelates enabled preoperative whole-body tumor detection by MRI, intraoperative guidance by real-time fluorescence, intraoperative histological analysis of margin status by fluorescence, and postoperative MRI tumor quantification. Animals whose tumors were resected with ACPPD guidance had better long-term tumor-free survival and overall survival than animals whose tumors were resected with traditional bright-field illumination only.


Url:
DOI: 10.1073/pnas.0910261107
PubMed: 20160097
PubMed Central: 2840114

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PMC:2840114

Le document en format XML

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<p>The completeness of tumor removal during surgery is dependent on the surgeon’s ability to differentiate tumor from normal tissue using subjective criteria that are not easily quantifiable. A way to objectively assess tumor margins during surgery in patients would be of great value. We have developed a method to visualize tumors during surgery using activatable cell-penetrating peptides (ACPPs), in which the fluorescently labeled, polycationic cell-penetrating peptide (CPP) is coupled via a cleavable linker to a neutralizing peptide. Upon exposure to proteases characteristic of tumor tissue, the linker is cleaved, dissociating the inhibitory peptide and allowing the CPP to bind to and enter tumor cells. In mice, xenografts stably transfected with green fluorescent protein show colocalization with the Cy5-labeled ACPPs. In the same mouse models, Cy5-labeled free ACPPs and ACPPs conjugated to dendrimers (ACPPDs) delineate the margin between tumor and adjacent tissue, resulting in improved precision of tumor resection. Surgery guided by ACPPD resulted in fewer residual cancer cells left in the animal after surgery as measured by Alu PCR. A single injection of ACPPD dually labeled with Cy5 and gadolinium chelates enabled preoperative whole-body tumor detection by MRI, intraoperative guidance by real-time fluorescence, intraoperative histological analysis of margin status by fluorescence, and postoperative MRI tumor quantification. Animals whose tumors were resected with ACPPD guidance had better long-term tumor-free survival and overall survival than animals whose tumors were resected with traditional bright-field illumination only.</p>
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<article-id pub-id-type="pmc">2840114</article-id>
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<article-title>Surgery with molecular fluorescence imaging using activatable cell-penetrating peptides decreases residual cancer and improves survival</article-title>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Nguyen</surname>
<given-names>Quyen T.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Olson</surname>
<given-names>Emilia S.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>b</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>c</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Aguilera</surname>
<given-names>Todd A.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>b</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>c</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jiang</surname>
<given-names>Tao</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>b</sup>
</xref>
<xref ref-type="aff" rid="aff5">
<sup>d</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Scadeng</surname>
<given-names>Miriam</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>e</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ellies</surname>
<given-names>Lesley G.</given-names>
</name>
<xref ref-type="aff" rid="aff6">
<sup>f</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tsien</surname>
<given-names>Roger Y.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>b</sup>
</xref>
<xref ref-type="aff" rid="aff5">
<sup>d</sup>
</xref>
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<sup>1</sup>
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<aff id="aff1">Departments of
<sup>a</sup>
Surgery,</aff>
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<sup>b</sup>
Pharmacology,</aff>
<aff id="aff3">
<sup>e</sup>
Radiology, and</aff>
<aff id="aff6">
<sup>f</sup>
Pathology,</aff>
<aff id="aff4">
<sup>c</sup>
Medical Scientist Training Program, and</aff>
<aff id="aff5">
<sup>d</sup>
Howard Hughes Medical Institute,
<institution>University of California at San Diego</institution>
, La Jolla, CA 92093-0647</aff>
</contrib-group>
<author-notes>
<corresp id="cor1">
<sup>1</sup>
To whom correspondence should be addressed. E-mail:
<email>rtsien@ucsd.edu</email>
.</corresp>
<fn fn-type="edited-by">
<p>Edited
<xref ref-type="fn" rid="fn1">*</xref>
by Robert Langer, Massachusetts Institute of Technology, Cambridge, MA, and approved December 24, 2009 (received for review September 9, 2009)</p>
</fn>
<fn fn-type="con">
<p>Author contributions: Q.T.N., E.S.O., T.A.A., and R.Y.T. designed research; Q.T.N., E.S.O., T.A.A., and M.S. performed research; T.J. and L.G.E. contributed new reagents/analytic tools; Q.T.N., E.S.O., T.A.A., and R.Y.T. analyzed data; and Q.T.N. and E.S.O. wrote the paper.</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>16</day>
<month>2</month>
<year>2010</year>
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<pub-date pub-type="ppub">
<day>2</day>
<month>3</month>
<year>2010</year>
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<month>2</month>
<year>2010</year>
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<pmc-comment> PMC Release delay is 0 months and 0 days and was based on the . </pmc-comment>
<volume>107</volume>
<issue>9</issue>
<fpage>4317</fpage>
<lpage>4322</lpage>
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<license-p>Freely available online through the PNAS open access option.</license-p>
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<abstract>
<p>The completeness of tumor removal during surgery is dependent on the surgeon’s ability to differentiate tumor from normal tissue using subjective criteria that are not easily quantifiable. A way to objectively assess tumor margins during surgery in patients would be of great value. We have developed a method to visualize tumors during surgery using activatable cell-penetrating peptides (ACPPs), in which the fluorescently labeled, polycationic cell-penetrating peptide (CPP) is coupled via a cleavable linker to a neutralizing peptide. Upon exposure to proteases characteristic of tumor tissue, the linker is cleaved, dissociating the inhibitory peptide and allowing the CPP to bind to and enter tumor cells. In mice, xenografts stably transfected with green fluorescent protein show colocalization with the Cy5-labeled ACPPs. In the same mouse models, Cy5-labeled free ACPPs and ACPPs conjugated to dendrimers (ACPPDs) delineate the margin between tumor and adjacent tissue, resulting in improved precision of tumor resection. Surgery guided by ACPPD resulted in fewer residual cancer cells left in the animal after surgery as measured by Alu PCR. A single injection of ACPPD dually labeled with Cy5 and gadolinium chelates enabled preoperative whole-body tumor detection by MRI, intraoperative guidance by real-time fluorescence, intraoperative histological analysis of margin status by fluorescence, and postoperative MRI tumor quantification. Animals whose tumors were resected with ACPPD guidance had better long-term tumor-free survival and overall survival than animals whose tumors were resected with traditional bright-field illumination only.</p>
</abstract>
<kwd-group>
<kwd>intraoperative fluorescence imaging</kwd>
<kwd>molecular navigation</kwd>
<kwd>long-term survival</kwd>
<kwd>molecular imaging</kwd>
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<name sortKey="Olson, Emilia S" sort="Olson, Emilia S" uniqKey="Olson E" first="Emilia S." last="Olson">Emilia S. Olson</name>
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