Prolyl isomerase Pin1 acts downstream of miR200c to promote cancer stem-like cell traits in breast cancer.

Abstract:

:Breast cancer stem-like cells (BCSC) have been implicated in tumor growth, metastasis, drug resistance, and relapse but druggable targets in appropriate subsets of this cell population have yet to be identified. Here we identify a fundamental role for the prolyl isomerase Pin1 in driving BCSC expansion, invasiveness, and tumorigenicity, defining it as a key target of miR200c, which is known to be a critical regulator in BCSC. Pin1 overexpression expanded the growth and tumorigenicity of BCSC and triggered epithelial-mesenchymal transition. Conversely, genetic or pharmacological inhibition of Pin1 reduced the abundance and self-renewal activity of BCSC. Moreover, moderate overexpression of miR200c-resistant Pin1 rescued the BCSC defect in miR200c-expressing cells. Genetic deletion of Pin1 also decreased the abundance and repopulating capability of normal mouse mammary stem cells. In human cells, freshly isolated from reduction mammoplasty tissues, Pin1 overexpression endowed BCSC traits to normal breast epithelial cells, expanding both luminal and basal/myoepithelial lineages in these cells. In contrast, Pin1 silencing in primary breast cancer cells freshly isolated from clinical samples inhibited the expansion, self-renewal activity, and tumorigenesis of BCSC in vitro and in vivo. Overall, our work demonstrated that Pin1 is a pivotal regulator acting downstream of miR200c to drive BCSC and breast tumorigenicity, highlighting a new therapeutic target to eradicate BCSC.

journal_name

Cancer Res

journal_title

Cancer research

authors

Luo ML,Gong C,Chen CH,Lee DY,Hu H,Huang P,Yao Y,Guo W,Reinhardt F,Wulf G,Lieberman J,Zhou XZ,Song E,Lu KP

doi

10.1158/0008-5472.CAN-13-2785

subject

Has Abstract

pub_date

2014-07-01 00:00:00

pages

3603-16

issue

13

eissn

0008-5472

issn

1538-7445

pii

0008-5472.CAN-13-2785

journal_volume

74

pub_type

杂志文章
  • Normal bronchial epithelial cell expression of glutathione transferase P1, glutathione transferase M3, and glutathione peroxidase is low in subjects with bronchogenic carcinoma.

    abstract::Normal bronchial epithelial cells (NBECs) are at risk for damage from inhaled and endogenous oxidative species and from epoxide metabolites of inhaled polycyclic aromatic hydrocarbons. Epidemiological and in vitro data suggest that interindividual variation in this risk may result from variation in NBEC expression of ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Crawford EL,Khuder SA,Durham SJ,Frampton M,Utell M,Thilly WG,Weaver DA,Ferencak WJ,Jennings CA,Hammersley JR,Olson DA,Willey JC

    更新日期:2000-03-15 00:00:00

  • Cytochrome P450c17alpha gene (CYP17) polymorphism predicts use of hormone replacement therapy.

    abstract::We investigated whether a polymorphism in the cytochrome P450c17alpha gene (CYP17), which is associated with higher endogenous hormone levels, influences the use of hormone replacement therapy (HRT). The study included 749 postmenopausal women ages 44-75 years at baseline randomly selected from a larger multiethnic co...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Feigelson HS,McKean-Cowdin R,Pike MC,Coetzee GA,Kolonel LN,Nomura AM,Le Marchand L,Henderson BE

    更新日期:1999-08-15 00:00:00

  • Frequent inactivation of PTEN/MMAC1 in primary prostate cancer.

    abstract::Sporadic prostate carcinoma is the most common male cancer in the Western world, yet many of the major genetic events involved in the progression of this often fatal cancer remain to be elucidated. Numerous cytogenetic and allelotype studies have reported frequent loss of heterozygosity on chromosomal arm 10q in spora...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Cairns P,Okami K,Halachmi S,Halachmi N,Esteller M,Herman JG,Jen J,Isaacs WB,Bova GS,Sidransky D

    更新日期:1997-11-15 00:00:00

  • A Model of Indirect Cell Death Caused by Tumor Vascular Damage after High-Dose Radiotherapy.

    abstract::There is increasing evidence that high doses of radiotherapy, like those delivered in stereotactic body radiotherapy (SBRT), trigger indirect mechanisms of cell death. Such effect seems to be two-fold. High doses may trigger an immune response and may cause vascular damage, leading to cell starvation and death. Develo...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-19-0181

    authors: Rodríguez-Barbeito P,Díaz-Botana P,Gago-Arias A,Feijoo M,Neira S,Guiu-Souto J,López-Pouso Ó,Gómez-Caamaño A,Pardo-Montero J

    更新日期:2019-12-01 00:00:00

  • Allelic loss at chromosome 3p characterizes clear cell phenotype of renal cell carcinoma.

    abstract::Incidence of the loss of heterozygosity on chromosome 3p was evaluated using 7 polymorphic probes in 35 Japanese patients with sporadic renal cell carcinoma (RCC). Overall frequency of the loss of heterozygosity on 3p was 53%, representing 16 of 30 informative cases. Examination of the relationship between histopathol...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Ogawa O,Kakehi Y,Ogawa K,Koshiba M,Sugiyama T,Yoshida O

    更新日期:1991-02-01 00:00:00

  • Proteasome function is required for DNA damage response and fanconi anemia pathway activation.

    abstract::Proteasome inhibitors sensitize tumor cells to DNA-damaging agents, including ionizing radiation (IR), and DNA cross-linking agents (melphalan and cisplatin) through unknown mechanisms. The Fanconi anemia pathway is a DNA damage-activated signaling pathway, which regulates cellular resistance to DNA cross-linking agen...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-07-1015

    authors: Jacquemont C,Taniguchi T

    更新日期:2007-08-01 00:00:00

  • Bcl2 is the guardian of microtubule integrity.

    abstract::We have investigated the ability of several drugs commonly used in the treatment of human cancer to induce bcl2 phosphorylation and cell death in human cell lines derived from acute leukemia, lymphoma, breast cancer, and prostate cancer. The results of this analysis indicate that drugs affecting the integrity of micro...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Haldar S,Basu A,Croce CM

    更新日期:1997-01-15 00:00:00

  • Potentiation of the antiangiogenic ability of linomide by androgen ablation involves down-regulation of vascular endothelial growth factor in human androgen-responsive prostatic cancers.

    abstract::Linomide is a p.o. active antiangiogenic agent that has been demonstrated to be effective in suppressing the in vivo growth of rat and human prostatic cancer xenografts. The present studies were conducted to determine whether the angiogenic molecules, vascular endothelial growth factor/vascular permeability factor (VE...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Joseph IB,Isaacs JT

    更新日期:1997-03-15 00:00:00

  • The suppression of drug-induced apoptosis by activation of v-ABL protein tyrosine kinase.

    abstract::Cells with a temperature-sensitive mutant of the v-abl oncoprotein (IC.DP) were treated with the anticancer drugs melphalan or hydroxyurea. At the restrictive temperature for v-ABL protein tyrosine kinase activity, drug-treated IC.DP cells died by apoptosis. In contrast, apoptotic cell death induced by either drug was...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Chapman RS,Whetton AD,Dive C

    更新日期:1994-10-01 00:00:00

  • Tumorigenicity of the cyc- variant of the S49 murine lymphoma deficient in the Gs-alpha subunit of adenylate cyclase.

    abstract::S49 cyc- lymphoma cells contain a mutation resulting in loss of a functional guanine nucleotide regulatory protein rendering their adenylate cyclase refractory to most stimuli. S49 wild-type and cyc- clones were used in the present study to investigate the possible association of altered cAMP metabolism with tumorigen...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Stadel JM,Johnson RK,Mirabelli CK,Powers DA,Sung CM,Faucette LF,McCabe FL,Crooke ST

    更新日期:1988-02-01 00:00:00

  • Mechanism of inhibition of cell proliferation by Vinca alkaloids.

    abstract::We have used a structure-activity approach to investigate whether the Vinca alkaloids inhibit cell proliferation primarily by means of their effects on mitotic spindle microtubules or by another mechanism or by a combination of mechanisms. Five Vinca alkaloids were used to investigate the relationship in HeLa cells be...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Jordan MA,Thrower D,Wilson L

    更新日期:1991-04-15 00:00:00

  • Carbamyl phosphate synthetases in rat liver neoplasms.

    abstract::Isozymes of carbamyl phosphate synthetase (CPS), CPS I, a mitochondrial enzyme found exclusively in liver and involved in urea synthesis, and of CPS II, a soluble cytoplasmic enzyme widely distributed in animal tissues, were assayed in rat liver and in a series of rat liver neoplasms ranging widely in growth rate and ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Lawson D,Paik WK,Morris HP,Weinhouse S

    更新日期:1975-01-01 00:00:00

  • Suppression of intracranial human glioma growth after intramuscular administration of an adeno-associated viral vector expressing angiostatin.

    abstract::Despite various therapeutic interventions, glioblastoma multiforme (GBM) is one of the most highly vascularized neoplasms in humans with poor prognosis. In this study, we show that a single i.m. injection of an adeno-associated viral (AAV) vector expressing angiostatin, a potent angiogenic inhibitor, effectively suppr...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Ma HI,Guo P,Li J,Lin SZ,Chiang YH,Xiao X,Cheng SY

    更新日期:2002-02-01 00:00:00

  • In vitro and in vivo antitumor effects of the dual insulin-like growth factor-I/insulin receptor inhibitor, BMS-554417.

    abstract::The insulin-like growth factor receptor (IGF-IR) and insulin receptor are either overactivated and/or overexpressed in a wide range of tumor types and contribute to tumorigenicity, proliferation, metastasis, and drug resistance. Here, we show that BMS-554417, a novel small molecule developed as an inhibitor of IGF-IR,...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-05-1107

    authors: Haluska P,Carboni JM,Loegering DA,Lee FY,Wittman M,Saulnier MG,Frennesson DB,Kalli KR,Conover CA,Attar RM,Kaufmann SH,Gottardis M,Erlichman C

    更新日期:2006-01-01 00:00:00

  • Phenotypic characterization of lung cancers in fine needle aspiration biopsies using monoclonal antibody B72.3.

    abstract::Monoclonal antibody B72.3, reactive with a high-molecular-weight glycoprotein tumor-associated antigen (designated TAG-72), has been previously shown to be reactive with formalin-fixed paraffin-embedded tissue sections of adenocarcinomas of the ovary, colon, and breast and not a variety of normal adult tissues. It has...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Johnston WW,Szpak CA,Thor A,Schlom J

    更新日期:1986-12-01 00:00:00

  • Requirements for and kinetics of growth arrest of neoplastic cells by confluent 10T1/2 fibroblasts induced by a specific inhibitor of cyclic adenosine 3':5'-phosphodiesterase.

    abstract::This study was conducted to further characterize the previously described phenomenon of growth inhibition of neoplastically transformed C3H/10T1/2 cells (T10T1/2) by nontransformed C3H/10T1/2 clone 8 mouse embryo fibroblast (10T1/2) cells in the presence of inhibitors of cyclic adenosine 3':5'-monophosphate (cAMP) pho...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Bertram JS,Faletto MB

    更新日期:1985-05-01 00:00:00

  • Identification of the human papillomavirus type 18 E6 and E6 proteins in nuclear protein fractions from human cervical carcinoma cells grown in the nude mouse or in vitro.

    abstract::We recently reported the transcription patterns of human papillomavirus (HPV) type 18 sequences in human cervical carcinoma cell lines. The open reading frames (ORFs) E6* and E6 represent the 5'-terminal cistrons in HPV18 mRNAs. ORF E6* was assumed to be specific for HPV types associated with genital carcinomas. To id...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Schneider-Gädicke A,Kaul S,Schwarz E,Gausepohl H,Frank R,Bastert G

    更新日期:1988-06-01 00:00:00

  • Glucose-regulated protein 78 controls cross-talk between apoptosis and autophagy to determine antiestrogen responsiveness.

    abstract::While more than 70% of breast cancers express estrogen receptor-α (ER+), endocrine therapies targeting these receptors often fail. The molecular mechanisms that underlie treatment resistance remain unclear. We investigated the potential role of glucose-regulated protein 78 (GRP78) in mediating estrogen resistance. Hum...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-12-0269

    authors: Cook KL,Shajahan AN,Wärri A,Jin L,Hilakivi-Clarke LA,Clarke R

    更新日期:2012-07-01 00:00:00

  • Physical and chemical modifications of adriamycin:iron complex by phospholipid bilayers.

    abstract::Adriamycin (ADM) and the ADM:Fe(III) complex both interact with phosphatidylcholine bilayers in aqueous vesicle dispersions. The immediate interaction of either ADM or ADM:Fe(III) with phospholipid causes little change in their absorption or emission spectra, but considerably increases the steady-state fluorescence an...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Samuni A,Chong PL,Barenholz Y,Thompson TE

    更新日期:1986-02-01 00:00:00

  • Binding analysis of the estrogen receptor to its specific DNA target site in human breast cancer.

    abstract::The estrogen receptor (ER) is a nuclear protein with a hormone- and a DNA-binding domain. We examined the DNA binding of ER in MCF-7 cells and 79 primary breast cancers by gel mobility shift assay using as a probe the estrogen response element (ERE). The mobility shift assay showed saturable, specific binding of ER to...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Foster BD,Cavener DR,Parl FF

    更新日期:1991-07-01 00:00:00

  • Growth regulation of human breast and ovarian tumor cells by heregulin: Evidence for the requirement of ErbB2 as a critical component in mediating heregulin responsiveness.

    abstract::Alterations in the expression of the epidermal growth factor (EGF) receptor ErbB family are frequently encountered in a number of human cancers. Two of these receptors, ErbB3 and ErbB4, are known to bind a family of related proteins termed heregulins (HRGs) or neu differentiation factors. In biologically relevant syst...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Lewis GD,Lofgren JA,McMurtrey AE,Nuijens A,Fendly BM,Bauer KD,Sliwkowski MX

    更新日期:1996-03-15 00:00:00

  • Thermal dosimetry and temperature measurements.

    abstract::A crucial ingredient of any hyperthermia procedure is the accurate measurement of achieved temperature. In this paper, we present some accuracy and resolution suggestions and address the problem of temperature measurements when electromagnetic energy is used as the mode of heating. In such cases, conventional metallic...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Christensen DA

    更新日期:1979-06-01 00:00:00

  • Novel Protein Disulfide Isomerase Inhibitor with Anticancer Activity in Multiple Myeloma.

    abstract::Multiple myeloma cells secrete more disulfide bond-rich proteins than any other mammalian cell. Thus, inhibition of protein disulfide isomerases (PDI) required for protein folding in the endoplasmic reticulum (ER) should increase ER stress beyond repair in this incurable cancer. Here, we report the mechanistically unb...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-15-3099

    authors: Vatolin S,Phillips JG,Jha BK,Govindgari S,Hu J,Grabowski D,Parker Y,Lindner DJ,Zhong F,Distelhorst CW,Smith MR,Cotta C,Xu Y,Chilakala S,Kuang RR,Tall S,Reu FJ

    更新日期:2016-06-01 00:00:00

  • Disposition and metabolism of 1-(tetrahydro-2-furanyl)-5-fluorouracil (ftorafur) in humans.

    abstract::The pharmacology of high-dose 1-(tetrahydro-2-furanyl)-5-fluorouracil (FT) has been studied by radiochemical and chromatographic techniques in eight patients. Plasma disappearance of FT was exponential, with a half-life of 8.8 hr. Plasma concentrations of 5-fluorouracil (FUra) were sustained at 12.8 nmol/ml (1.7 micro...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Benvenuto JA,Lu K,Hall SW,Benjamin RS,Loo TL

    更新日期:1978-11-01 00:00:00

  • Enhanced polyglutamylation of aminopterin relative to methotrexate in the Ehrlich ascites tumor cell in vitro.

    abstract::The polyglutamylation of aminopterin and methotrexate (N10-methylaminopterin) was compared in the Ehrlich ascites tumor in vitro. Three poly-gamma-glutamyl conjugates of methotrexate and aminopterin were detected, although at an equal (1 microM) extracellular drug concentration, the net accumulation of aminopterin pol...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Matherly LH,Voss MK,Anderson LA,Fry DW,Goldman ID

    更新日期:1985-03-01 00:00:00

  • Role of amino acid depletion in combined treatment of neoplastic cells with methotrexate and L-asparaginase.

    abstract::The effect of pretreatment with L-asparaginase on the cytotoxicity of methotrexate (MTX) was studied in L5178Y murine leukemic cells and L-929 cells grown in vitro. The results were correlated with the effects of L-asparaginase on DNA synthesis. At low concentrations of the enzyme, pretreatment of cells enhanced the e...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Chlopkiewicz B,Koziorowska J

    更新日期:1975-06-01 00:00:00

  • Silencing of p29 affects DNA damage responses with UV irradiation.

    abstract::Human p29 is a newly identified nuclear protein whose function is largely undetermined. We found that p29 associated with chromatin, interacted with MCM3, and localized with proliferating cell nuclear antigen foci in the S phase. Silencing of p29 using small interfering RNA duplexes reduced DNA synthesis and increased...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-05-3229

    authors: Chu PC,Yang YC,Lu YT,Chen HT,Yu LC,Chang MS

    更新日期:2006-09-01 00:00:00

  • E-cadherin expression in human breast cancer cells suppresses the development of osteolytic bone metastases in an experimental metastasis model.

    abstract::The molecular mechanisms by which human cancer cells spread to bone are largely unexplored. The process likely involves cell adhesion molecules (CAMs) that are responsible for homophilic and heterophilic cell-cell interactions. One relevant CAM may be the calcium-dependent transmembrane glycoprotein E-cadherin. To inv...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Mbalaviele G,Dunstan CR,Sasaki A,Williams PJ,Mundy GR,Yoneda T

    更新日期:1996-09-01 00:00:00

  • Gefitinib reverses TRAIL resistance in human bladder cancer cell lines via inhibition of AKT-mediated X-linked inhibitor of apoptosis protein expression.

    abstract::In a previous study, we found that the small-molecule epidermal growth factor receptor (EGFR) inhibitor gefitinib (ZD1839, Iressa) blocked cell proliferation at biologically relevant concentrations in approximately one third (6 of 17) of human bladder cancer cell lines examined. Here, we studied the effects of gefitin...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-06-1224

    authors: Shrader M,Pino MS,Lashinger L,Bar-Eli M,Adam L,Dinney CP,McConkey DJ

    更新日期:2007-02-15 00:00:00

  • Delayed sensitization to heat by inhibitors of polyamine-biosynthetic enzymes.

    abstract::Exposure of Chinese hamster ovary cells to the enzyme inhibitors methylglyoxal bis(guanylhydrazone and alpha-difluoromethylornithine (DFMO) results in increased sensitivity to hyperthermia. While methylglyoxal bis(guanylhydrazone) demonstrates pronounced cytotoxicity at moderate extracellular concentrations, DFMO is t...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Fuller DJ,Gerner EW

    更新日期:1982-12-01 00:00:00