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      AND-gate contrast agents for enhanced fluorescence-guided surgery

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          Abstract

          The surgical resection of tumours requires the precise location and definition of the margins between lesions and normal tissue. However, this is made difficult by irregular margin borders. Although molecularly targeted optical contrast agents can be used to define tumour margins during surgery in real time, the selectivity of the contrast agents is often limited by the target being expressed in both healthy and tumour tissues. Here, we show that AND-gate optical imaging probes requiring the processing of two substrates by multiple tumour-specific enzymes produce a fluorescent signal with significantly improved specificity and sensitivity to tumour tissue. We evaluated the performance of the probes in mouse models of mammary tumours and of metastatic lung cancer, and during fluorescence-guided robotic surgery. Imaging probes relying on multivariate activation to selectively target complex patterns of enzymatic activity should be useful in disease detection, treatment and monitoring.

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          Most cited references51

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          Innate and adaptive immune cells in the tumor microenvironment.

          Most tumor cells express antigens that can mediate recognition by host CD8(+) T cells. Cancers that are detected clinically must have evaded antitumor immune responses to grow progressively. Recent work has suggested two broad categories of tumor escape based on cellular and molecular characteristics of the tumor microenvironment. One major subset shows a T cell-inflamed phenotype consisting of infiltrating T cells, a broad chemokine profile and a type I interferon signature indicative of innate immune activation. These tumors appear to resist immune attack through the dominant inhibitory effects of immune system-suppressive pathways. The other major phenotype lacks this T cell-inflamed phenotype and appears to resist immune attack through immune system exclusion or ignorance. These two major phenotypes of tumor microenvironment may require distinct immunotherapeutic interventions for maximal therapeutic effect.
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            New functions for the matrix metalloproteinases in cancer progression.

            Matrix metalloproteinases (MMPs) have long been associated with cancer-cell invasion and metastasis. This provided the rationale for clinical trials of MMP inhibitors, unfortunately with disappointing results. We now know, however, that the MMPs have functions other than promotion of invasion, have substrates other than components of the extracellular matrix, and that they function before invasion in the development of cancer. With this knowledge in hand, can we rethink the use of MMP inhibitors in the clinic?
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              1423 pancreaticoduodenectomies for pancreatic cancer: A single-institution experience.

              Pancreaticoduodenectomy (PD) with the possible addition of neoadjuvant or adjuvant therapy is the standard of care in the United States for adenocarcinoma originating in the pancreatic head, neck, and uncinate process. We reviewed 1423 patients who underwent a PD for a malignancy originating in the pancreas at our institution between 1970 and 2006. We examined 1175 PDs for ductal adenocarcinomas in greater detail. Eighteen different histological types of pancreatic cancer were identified; the most common diagnoses included ductal adenocarcinoma, neuroendocrine carcinoma, and IPMN with invasive cancer. Patients with ductal adenocarcinoma were analyzed in detail. The median age was 66 years, with patients in the present decade significantly older (68 years), on average, than patients in the three prior decades (e.g., 60 years in 1970, P = 0.02). The median tumor diameter was 3 cm; 42% of the resections had positive margins and 78% had positive lymph nodes. The perioperative morbidity was 38%. The median postoperative stay declined over time, from 16 days in the 1980s to 8 days in the 2000s (P < 0.001). The perioperative mortality declined from 30% in the 1970s to 1% in the 2000s (P < 0.001). The median survival for all patients with ductal adenocarcinoma was 18 months (1-year survival = 65 %, 2-year survival = 37%, 5-year survival = 18%). In a Cox proportional hazards model, pathological factors having a significant impact on survival included tumor diameter, resection margin status, lymph node status, and histologic grade. This is the largest single-institution experience with PD for pancreatic cancer. Patients who have cancers with favorable pathological features have a statistically significant improved long-term survival.
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                Author and article information

                Journal
                101696896
                45929
                Nat Biomed Eng
                Nat Biomed Eng
                Nature biomedical engineering
                2157-846X
                10 September 2020
                28 September 2020
                March 2021
                28 March 2021
                : 5
                : 3
                : 264-277
                Affiliations
                [1 ]Department of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, California, USA
                [2 ]Department of Chemical and Systems Biology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, California, USA
                [3 ]Department of Microbiology and Immunology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, California, USA
                [4 ]Department of Comparative Medicine, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, California, USA
                [5 ]Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, California, USA
                [6 ]Department of Radiology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, California, USA
                [7 ]Intuitive Surgical Inc., 1020 Kifer Road, Sunnyvale, California 94086, United States
                Author notes

                Author contributions

                M.B. and J.C.W conceived of the AND-Gate probe concept and designed all experiments. J.C.W synthesized all AND-Gate probes, conducted the fluorogenic substrate assays, live and fixed cell fluorescent microscopy experiments, and mouse model experiments. J.C.W and M.B. wrote the text of the paper and constructed the figures with input from J.J.Y. and K.C.M. M.T. and J.J.Y helped perform live and ex vivo imaging during the 4T1 cancer mouse model experiment including dissection of the mice. M.T. aided in the immunohistochemical analysis of 4T1 tumors. A.A, A.K., and J.S. assisted with the robotic surgery. K.M.C. evaluated H&E sections for the colorectal and 4T1 breast cancer mouse models.

                [* ] Correspondence and requests for materials should be addressed to mbogyo@ 123456stanford.edu
                Article
                NIHMS1624234
                10.1038/s41551-020-00616-6
                7969380
                32989286
                c8ffa104-eb08-4263-8195-9545b6d830e9

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                Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

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