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  1. Article ; Online: Cervical Cancer Stage at Diagnosis and Survival among Women ≥65 Years in California.

    Cooley, Julianne J P / Maguire, Frances B / Morris, Cyllene R / Parikh-Patel, Arti / Abrahão, Renata / Chen, Hui A / Keegan, Theresa H M

    Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology

    2023  Volume 32, Issue 1, Page(s) 91–97

    Abstract: Background: Through adequate screening and follow-up, cervical cancer can be prevented or detected at early-stage (stage I), which is related to excellent survival. Current guidelines recommend discontinuing screening for women ≥65 years with history of ...

    Abstract Background: Through adequate screening and follow-up, cervical cancer can be prevented or detected at early-stage (stage I), which is related to excellent survival. Current guidelines recommend discontinuing screening for women ≥65 years with history of normal Pap and/or HPV tests, potentially leaving this age group vulnerable. This study examined late-stage disease in a population-based cohort.
    Methods: Using California Cancer Registry data, we identified 12,442 patients ages ≥21 years with a first primary cervical cancer diagnosed during 2009-2018. Proportions of late-stage disease (stages II-IV) and early- and late-stage 5-year relative survival are presented by the age group. Among patients ages ≥65 years, multivariable logistic regression estimated associations of sociodemographic and clinical characteristics with late-stage cervical cancer.
    Results: Nearly one fifth of patients (n = 2,171, 17.4%) were ≥65 years. More women ages ≥65 years (71%) presented with late-stage disease than younger women (48% in patients ages <65). Late-stage 5-year relative survival was lower for women ≥65 years (23.2%-36.8%) compared with patients <65 (41.5%-51.5%). Characteristics associated with late-stage cervical cancer in women ≥65 years included older age [odds ratio (OR), 1.02; 95% confidence interval (CI), 1.01-1.04; each year], non-adenocarcinoma histologic subtypes, and comorbidities (OR, 1.59; 95% CI, 1.21-2.08).
    Conclusions: There remains a significant burden of advanced cervical cancer in women ≥65.
    Impact: Efforts should be made to better understand how the current screening paradigm is failing women of 65 years and older. Future work should focus on determining past screening history, lapses in follow-up care, and non-invasive testing approaches.
    MeSH term(s) Humans ; Female ; Young Adult ; Adult ; Aged ; Uterine Cervical Neoplasms/diagnosis ; Uterine Cervical Neoplasms/epidemiology ; Uterine Cervical Neoplasms/pathology ; Vaginal Smears ; Papanicolaou Test ; Mass Screening ; Registries ; Papillomavirus Infections/diagnosis ; Papillomavirus Infections/epidemiology ; Papillomavirus Infections/complications ; California/epidemiology ; Early Detection of Cancer
    Language English
    Publishing date 2023-01-08
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S. ; Research Support, N.I.H., Extramural
    ZDB-ID 1153420-5
    ISSN 1538-7755 ; 1055-9965
    ISSN (online) 1538-7755
    ISSN 1055-9965
    DOI 10.1158/1055-9965.EPI-22-0793
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: C3d-Targeted factor H inhibits tissue complement in disease models and reduces glomerular injury without affecting circulating complement.

    Liu, Fei / Ryan, Sarah T / Fahnoe, Kelly C / Morgan, Jennifer G / Cheung, Anne E / Storek, Michael J / Best, Alejandro / Chen, Hui A / Locatelli, Monica / Xu, Shuyun / Schmidt, Enno / Schmidt-Jiménez, Leon F / Bieber, Katja / Henderson, Joel M / Lian, Christine G / Verschoor, Admar / Ludwig, Ralf J / Benigni, Ariela / Remuzzi, Giuseppe /
    Salant, David J / Kalled, Susan L / Thurman, Joshua M / Holers, V Michael / Violette, Shelia M / Wawersik, Stefan

    Molecular therapy : the journal of the American Society of Gene Therapy

    2024  Volume 32, Issue 4, Page(s) 1061–1079

    Abstract: Complement-mediated diseases can be treated using systemic inhibitors. However, complement components are abundant in circulation, affecting systemic inhibitors' exposure and efficacy. Furthermore, because of complement's essential role in immunity, ... ...

    Abstract Complement-mediated diseases can be treated using systemic inhibitors. However, complement components are abundant in circulation, affecting systemic inhibitors' exposure and efficacy. Furthermore, because of complement's essential role in immunity, systemic treatments raise infection risk in patients. To address these challenges, we developed antibody fusion proteins combining the alternative-pathway complement inhibitor factor H (fH
    MeSH term(s) Humans ; Mice ; Rats ; Animals ; Complement Factor H/genetics ; Complement C3d/metabolism ; Kidney Diseases/etiology ; Antibodies ; Complement Activation
    Chemical Substances Complement Factor H (80295-65-4) ; Complement C3d (80295-45-0) ; Antibodies
    Language English
    Publishing date 2024-02-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2010592-7
    ISSN 1525-0024 ; 1525-0016
    ISSN (online) 1525-0024
    ISSN 1525-0016
    DOI 10.1016/j.ymthe.2024.02.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Non-muscle myosin-IIA is critical for podocyte f-actin organization, contractility, and attenuation of cell motility.

    Bondzie, Philip A / Chen, Hui A / Cao, Mei Zhen / Tomolonis, Julie A / He, Fangfang / Pollak, Martin R / Henderson, Joel M

    Cytoskeleton (Hoboken, N.J.)

    2016  Volume 73, Issue 8, Page(s) 377–395

    Abstract: Several glomerular pathologies resulting from podocyte injury are linked to genetic variation involving the MYH9 gene, which encodes the heavy chain of non-muscle myosin-IIA (NM-IIA). However, the functional role of NM-IIA has not been studied ... ...

    Abstract Several glomerular pathologies resulting from podocyte injury are linked to genetic variation involving the MYH9 gene, which encodes the heavy chain of non-muscle myosin-IIA (NM-IIA). However, the functional role of NM-IIA has not been studied extensively in podocytes. We hypothesized that NM-IIA is critical for maintenance of podocyte structure and mechanical function. To test this hypothesis, we studied murine podocytes in vitro subjected to blebbistatin inhibition of NM-II activity, or RNA interference-mediated, isoform-specific ablation of Myh9 gene and protein (NM-IIA) or its paralog Myh10 gene and protein (NM-IIB). Using quantitative immunofluorescence microscopy, traction force microscopy, and attachment and "wound healing" assays, we found that NM-IIA ablation altered podocyte actin cytoskeletal structure and focal adhesion distribution, decreased cell attachment and contractility, and increased cell motility. Blebbistatin treatment had similar effects. NM-IIB ablation produced cells that exhibited poor attachment, but cytoskeletal structural organization, contractility and motility were maintained. These findings indicate that NM-IIA is essential for maintenance of podocyte cytoskeletal structure and mechanical function in vitro, and NM-IIB does not replace it in this role when NM-IIA expression is altered. We conclude that critical podocyte functions may be affected by MYH9 mutations or disease-associated haplotypes. © 2016 Wiley Periodicals, Inc.
    MeSH term(s) Actin Cytoskeleton/metabolism ; Actins/metabolism ; Cell Movement ; Humans ; Muscle Contraction ; Nonmuscle Myosin Type IIA/metabolism ; Podocytes/metabolism ; Podocytes/pathology
    Chemical Substances Actins ; Nonmuscle Myosin Type IIA (EC 3.6.1.-)
    Language English
    Publishing date 2016-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2534372-5
    ISSN 1949-3592 ; 1949-3584
    ISSN (online) 1949-3592
    ISSN 1949-3584
    DOI 10.1002/cm.21313
    Database MEDical Literature Analysis and Retrieval System OnLINE

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