INGRID PAMELA Ehrenfeld Slater

Dr. INGRID PAMELA Ehrenfeld Slater

orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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22 June 2017 in Expert Opinion on Therapeutic Targets
Verified
Journal Article
Closed access
LMLuis Molina
Luis Molina
CFCarlos D. Figueroa
Carlos D. Figueroa
KBKanti D. Bhoola
Kanti D. Bhoola
ISINGRID PAMELA Ehrenfeld Slater
INGRID PAMELA Ehrenfeld Slater
Introduction: Breast cancer is clinically classified as ‘estrogen-positive’ when at least 1% of cancer cells stain for the estrogen receptor alpha (ERα). However, recent research on both basic and clinical aspects of breast cancer suggests that GPER-1 (G protein-coupled estrogen receptor-1) may have an important role in breast cancer. Areas covered: This review provides a comprehensive and systematic literature search on GPER-1. We have focused on the role of GPER-1 in breast cancer and on resistance to endocrine therapy, an unsolved clinical issue still under discussion. Expert opinion: The discovery of GPER-1 as a novel estrogen receptor is unique and the signaling pathways activated by its stimulation, when compared to the classical nuclear ERα, indicate a potential role of GPER-1 in the genesis and mechanisms of drug resistance in breast cancer. Tumors expressing ERα represent the largest group of breast cancer patients indicating that more women eventually die from ERα-positive breast tumors than from other more malignant breast cancer subtypes such as HER2-positive and the triple negative groups. It is important to develop new strategies on endocrine therapy with regard to ERα and GPER-1 receptors to achieve innovative successful therapeutic tools.

23 June 2020 in Frontiers in Cellular Neuroscience
Verified
Journal Article
Open access
CMCinthia Mella
Cinthia Mella
CFCarlos D. Figueroa
Carlos D. Figueroa
COCarola Otth
Carola Otth
ISINGRID PAMELA Ehrenfeld Slater
INGRID PAMELA Ehrenfeld Slater
Kallikrein-related peptidases (KLKs) are a family of serine proteases that when dysregulated may contribute to neuroinflammation and neurodegeneration. In the present review, we describe what is known about their physiological and pathological roles with an emphasis on KLK6 and KLK8, two KLKs that are highly expressed in the adult central nervous system (CNS). Altered expression and activity of KLK6 have been linked to brain physiology and the development of multiple sclerosis. On the other hand, altered levels of KLK6 in the brain and serum of people affected by Alzheimer's disease and Parkinson’s disease have been documented, pointing out to its function in amyloid metabolism and development of synucleinopathies. People who have structural genetic variants of KLK8 can suffer mental illnesses such as intellectual and learning disabilities, seizures and autism. Increased expression of KLK8 has also been implicated in schizophrenia, bipolar disorder, and depression. In addition, we discuss the possible link that exists between KLKs activity and certain viral infections that can affect the nervous system. Although little is known about the exact mechanisms that mediate KLKs function and their participation in neuroinflammatory and neurodegenerative disorders will open a new field to develop novel therapies to modulate their levels and/or activity and their harmful effects on the CNS.

28 January 2009 in Breast Cancer Research and Treatment
Verified
Journal Article
Closed access
PDF file
LMLuis Molina
Luis Molina
CMCarola E. Matus
Carola E. Matus
AAAngel Astroza
Angel Astroza
FPFrancisca Pavicic
Francisca Pavicic
ETEugenio Tapia
Eugenio Tapia
MPMaria T. Poblete
Maria T. Poblete

13 December 2018 in Clinical Science
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Journal Article
Closed access
PDF file
LMLuis Molina
Luis Molina
FBFelipe A. Bustamante
Felipe A. Bustamante
KBKanti D. Bhoola
Kanti D. Bhoola
CFCarlos D Figueroa
Carlos D Figueroa
ISINGRID PAMELA Ehrenfeld Slater
INGRID PAMELA Ehrenfeld Slater
Estrogens generated within endocrine organs and the reproductive system act as ligands for at least three types of estrogen receptors. Estrogen receptors α (ERα) and β (ERβ) belong to the so-called classical family of estrogen receptors, whereas the G protein-coupled receptor GPR30, also known as GPER-1, has been described as a novel estrogen receptor sited in the cell membrane of target cells. Furthermore, these receptors are under stimulation of a family of exogenous estrogens, known as phytoestrogens, which are a diverse group of non-steroidal plant compounds derived from plant food consumed by humans and animals. Because phytoestrogens are omnipresent in our daily diet, they are becoming increasingly important in both human health and disease. Recent evidence indicates that in addition to classical estrogen receptors, phytoestrogens also activate GPER-1 a relevant observation since GPER-1 is involved in several physiopathological disorders and especially in estrogen-dependent diseases such as breast cancer. The first estrogen receptors discovered were the classical ERα and ERβ, but from an evolutionary point of view G protein-coupled receptors trace their origins in history to over a billion years ago suggesting that estrogen receptors like GPER-1 may have been the targets of choice for ancient phytoestrogens and/or estrogens. This review provides a comprehensive and systematic literature search on phytoestrogens and its relationship with classical estrogen receptors and GPER-1 including its role in breast cancer, an issue still under discussion.

1 February 2021 in Archives of Oral Biology
Verified
Journal Article
Closed access
DVDiego Vergara-Llanos
Diego Vergara-Llanos
TKTania Koning
Tania Koning
MPMaria Francisca Pavicic
Maria Francisca Pavicic
Helia Bello-ToledoHelia Bello-Toledo
Helia Bello-Toledo
AGAndrés Díaz Gómez
Andrés Díaz Gómez
GSGabriela Sánchez-Sanhueza
Gabriela Sánchez-Sanhueza

13 December 2010 in Cancer Letters
Verified
Journal Article
Closed access
ISINGRID PAMELA Ehrenfeld Slater
INGRID PAMELA Ehrenfeld Slater
ICIvan Conejeros
Ivan Conejeros
MPMaria F. Pavicic
Maria F. Pavicic
CMCarola E. Matus
Carola E. Matus
CGCarlos B. Gonzalez
Carlos B. Gonzalez
CFCarlos D. Figueroa
Carlos D. Figueroa