Catherine Sherwin

Prof. Dr. Catherine Sherwin

Department of Pediatrics, Wright State University, Boonshoft School of Medicine, Dayton Children's Hospital, One Children's Plaza, Dayton, OH 45404-1815, USA

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 January 2020 in Frontiers in Pharmacology
Verified
Journal Article
Open access
PDF file
SISílvia M. Illamola
Sílvia M. Illamola
OAOgochukwu U. Amaeze
Ogochukwu U. Amaeze
LKLubov V. Krepkova
Lubov V. Krepkova
ABAngela K. Birnbaum
Angela K. Birnbaum
AKAshwin Karanam
Ashwin Karanam
Elena Y EnioutinaElena Y Enioutina
Elena Y Enioutina
About 80% of the consumers worldwide use herbal medicine (HMs) or other natural products. The percentage may vary significantly (7%–55%) among pregnant women, depending upon social status, ethnicity, and cultural traditions. This manuscript discusses the most common HMs used by pregnant women, and the potential interactions of HMs with conventional drugs in some medical conditions that occur during pregnancy (e.g., hypertension, asthma, epilepsy). It also includes an examination of the characteristics of pregnant HM consumers, the primary conditions for which HMs are taken, and a discussion related to the potential toxicity of HMs taken during pregnancy. Many cultures have used HMs in pregnancy to improve wellbeing of the mother and/or baby, or to help decrease nausea and vomiting, treat infection, ease gastrointestinal problems, prepare for labor, induce labor, or ease labor pains. One of the reasons why pregnant women use HMs is an assumption that HMs are safer than conventional medicine. However, for pregnant women with pre-existing conditions like epilepsy and asthma, supplementation of conventional treatment with HMs may further complicate their care. The use of HMs is frequently not reported to healthcare professionals. Providers are often not questioning HM use, despite little being known about the HM safety and HM-drug interactions during pregnancy. This lack of knowledge on potential toxicity and the ability to interact with conventional treatments may impact both mother and fetus. There is a need for education of women and their healthcare professionals to move away from the idea of HMs not being harmful. Healthcare professionals need to question women on whether they use any HMs or natural products during pregnancy, especially when conventional treatment is less efficient and/or adverse events have occurred as herbal-drug interactions could be the reason for these observations. Additionally, more preclinical and clinical studies are needed to evaluate HM efficacy and toxicity.

1 February 2012 in Clinical Pharmacokinetics
Verified
Journal Article
Closed access
PDF file
RCRoosmarijn F. W. De Cock
Roosmarijn F. W. De Cock
Karel AllegaertKarel Allegaert
Karel Allegaert
MSMichiel F. Schreuder
Michiel F. Schreuder
Catherine SherwinCatherine Sherwin
Catherine Sherwin
MHMatthijs de Hoog
Matthijs de Hoog
CKCatherijne A. J. Knibbe
Catherijne A. J. Knibbe

24 October 2019 in Cancers
Verified
Journal Article
Open access
PDF file
ATAnita Thyagarajan
Anita Thyagarajan
MAMamdouh Salman A. Alshehri
Mamdouh Salman A. Alshehri
KMKelly L.R. Miller
Kelly L.R. Miller
Catherine SherwinCatherine Sherwin
Catherine Sherwin
Jeffrey Bryant B TraversJeffrey Bryant B Travers
Jeffrey Bryant B Travers
Ravi SahuRavi Sahu
Ravi Sahu
Pancreatic ductal adenocarcinoma (PDAC) remains a devastating human malignancy with poor prognosis and low survival rates. Several cellular mechanisms have been linked with pancreatic carcinogenesis and also implicated in inducing tumor resistance to known therapeutic regimens. Of various factors, immune evasion mechanisms play critical roles in tumor progression and impeding the efficacy of cancer therapies including PDAC. Among immunosuppressive cell types, myeloid-derived suppressor cells (MDSCs) have been extensively studied and demonstrated to not only support PDAC development but also hamper the anti-tumor immune responses elicited by therapeutic agents. Notably, recent efforts have been directed in devising novel approaches to target MDSCs to limit their effects. Multiple strategies including immune-based approaches have been explored either alone or in combination with therapeutic agents to target MDSCs in preclinical and clinical settings of PDAC. The current review highlights the roles and mechanisms of MDSCs as well as the implications of this immunomodulatory cell type as a potential target to improve the efficacy of therapeutic regimens for PDAC.

1 June 2020 in Pediatric Drugs
Verified
Journal Article
Closed access
PDF file
JRJahidur Rashid
Jahidur Rashid
SKShaun S. Kumar
Shaun S. Kumar
KJKathleen M. Job
Kathleen M. Job
XLXiaoxi Liu
Xiaoxi Liu
CFCandice D. Fike
Candice D. Fike
Catherine SherwinCatherine Sherwin
Catherine Sherwin

15 December 2016 in Expert Review of Clinical Pharmacology
Verified
Journal Article
Closed access
EEElena Yu. Enioutina
Elena Yu. Enioutina
ESEmma R. Salis
Emma R. Salis
Kathleen JobKathleen Job
Kathleen Job
MGMichael I. Gubarev
Michael I. Gubarev
LKLubov V. Krepkova
Lubov V. Krepkova
Catherine SherwinCatherine Sherwin
Catherine Sherwin
Herbal medicine (HM) use is growing worldwide. Single herb preparations, ethnic and modern HM formulations are widely used as adjunct therapies or to improve consumer wellbeing. Areas covered: This final part in the publication series summarizes common tendencies in HM use as adjunct or alternative medicine, education of healthcare professionals and consumers, current and proposed guidelines regulating of production. We discuss potential HM-HM and HM-drug interactions that could lead to severe adverse events in situations where HMs are taken without proper medical professional oversight. Expert commentary: A number of serious problems have arisen with the steady global increase in HM use. HM interaction with conventional drugs (CD) may result in inadequate dosing of CD or adverse reactions; HM-HM interaction within herbal supplements could lead to toxicity of formulations. Inadequate education of clinicians and patients regarding medicinal properties of HMs must be addressed regionally and globally to ensure consumer safety.

25 September 2013 in Pharmaceutical Research
Verified
Journal Article
Closed access
PDF file
RCRoosmarijn F. W. De Cock
Roosmarijn F. W. De Cock
Karel AllegaertKarel Allegaert
Karel Allegaert
Catherine SherwinCatherine Sherwin
Catherine Sherwin
ENElisabet I. Nielsen
Elisabet I. Nielsen
MHMatthijs de Hoog
Matthijs de Hoog
CKCatherijne A. J. Knibbe
Catherijne A. J. Knibbe