PML nuclear bodies are general targets for inflammation and cell proliferation.

Abstract:

:Acute promyelocytic leukemia is associated with a t(15;17) translocation that generates a fusion product between PML and the retinoic acid receptor alpha. Recently, PML was shown to concentrate within subnuclear domains, referred to as nuclear bodies, that are disorganized in acute promyelocytic leukemia cells. This observation provided the first evidence that alteration of a nuclear structure may play a role in human pathogenesis. In an attempt to clarify the role of PML and, more generally, of the associated nuclear bodies, we used immunohistochemistry to explore the expression of PML in normal, inflammatory, and neoplastic human tissues. With the exception of endothelial cells and macrophages that contain a high amount of PML protein, a weak speckled labeling pattern was observed in the nucleus of all cell types analyzed. By contrast to normal tissues, the level of PML expression was considerably enhanced in inflammatory tissues, predominantly around the mononuclear cell infiltrate, as well as during either normal or pathological proliferative states, in particular in tumoral pathology. Surprisingly, in most hepatocellular carcinoma, a cytoplasmic delocalization of PML was observed. Finally, the number of PML nuclear bodies increased up to twice their normal value as quiescent cultured cells were stimulated to grow upon serum addition. Altogether these results strongly suggest that the PML-associated nuclear bodies are implicated both in the inflammatory process and in cell growth control.

journal_name

Cancer Res

journal_title

Cancer research

authors

Terris B,Baldin V,Dubois S,Degott C,Flejou JF,Hénin D,Dejean A

subject

Has Abstract

pub_date

1995-04-01 00:00:00

pages

1590-7

issue

7

eissn

0008-5472

issn

1538-7445

journal_volume

55

pub_type

杂志文章
  • Lethal and cytokinetic effects of anguidine on a human colon cancer cell line.

    abstract::Anguidine is a fungal metabolite with antitumor activity in a murine colon cancer model. Because of disappointing results in clinical trials, we analyzed the lethal and cytokinetic effects of anguidine on cultured human colon cancer cells. The studies revealed a moderate reduction in survival only after prolonged drug...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Dosik GM,Barlogie B,Johnston DA,Murphy WK,Drewinko B

    更新日期:1978-10-01 00:00:00

  • Aerobic glycolysis suppresses p53 activity to provide selective protection from apoptosis upon loss of growth signals or inhibition of BCR-Abl.

    abstract::Unlike the growth factor dependence of normal cells, cancer cells can maintain growth factor-independent glycolysis and survival through expression of oncogenic kinases, such as BCR-Abl. Although targeted kinase inhibition can promote cancer cell death, therapeutic resistance develops frequently, and further mechanist...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-10-0608

    authors: Mason EF,Zhao Y,Goraksha-Hicks P,Coloff JL,Gannon H,Jones SN,Rathmell JC

    更新日期:2010-10-15 00:00:00

  • Structure and possible mechanisms of TEL-AML1 gene fusions in childhood acute lymphoblastic leukemia.

    abstract::TEL-AML1 gene fusion derived by chromosomal translocation is a common acquired genetic lesion in pediatric cancer that is present in approximately 25% of B-cell precursor acute lymphoblastic leukemias, and recent evidence suggests that this recombination event may initiate leukemogenesis prenatally during fetal hemopo...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Wiemels JL,Greaves M

    更新日期:1999-08-15 00:00:00

  • Differential cell photosensitivity following porphyrin photodynamic therapy.

    abstract::Experiments were performed to determine if differences in porphyrin photosensitivity could be observed for cells with varying efficiency in DNA damage repair, as well as for cells which make up components of the vasculature. Photofrin II is undergoing current clinical evaluation for photodynamic therapy of solid tumor...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Gomer CJ,Rucker N,Murphree AL

    更新日期:1988-08-15 00:00:00

  • A unique structure for epidermal growth factor receptor bound to GW572016 (Lapatinib): relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells.

    abstract::GW572016 (Lapatinib) is a tyrosine kinase inhibitor in clinical development for cancer that is a potent dual inhibitor of epidermal growth factor receptor (EGFR, ErbB-1) and ErbB-2. We determined the crystal structure of EGFR bound to GW572016. The compound is bound to an inactive-like conformation of EGFR that is ver...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-04-1168

    authors: Wood ER,Truesdale AT,McDonald OB,Yuan D,Hassell A,Dickerson SH,Ellis B,Pennisi C,Horne E,Lackey K,Alligood KJ,Rusnak DW,Gilmer TM,Shewchuk L

    更新日期:2004-09-15 00:00:00

  • Genistein exerts multiple suppressive effects on human breast carcinoma cells.

    abstract::Dietary genistein, a natural flavone compound found in soy, has been proposed to be responsible for the low rate of breast cancer in Asian women. The cellular mechanisms of genistein's chemopreventive effects in vio have been largely unexplored. In our previous studies, we found that genistein exerted pronounced antip...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Shao ZM,Wu J,Shen ZZ,Barsky SH

    更新日期:1998-11-01 00:00:00

  • Activity of a novel 4-quinolinecarboxylic acid, NSC 368390 [6-fluoro-2-(2'-fluoro-1,1'-biphenyl-4-yl)-3-methyl-4-quinolinecarb oxylic acid sodium salt], against experimental tumors.

    abstract::A novel, substituted 4-quinolinecarboxylic acid (NSC 339768) demonstrated antitumor activity against L1210 leukemia and B16 melanoma in the National Cancer Institute's Developmental Therapeutics Program. An extensive analogue synthesis program was initiated; over 200 derivatives were synthesized and tested for antican...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Dexter DL,Hesson DP,Ardecky RJ,Rao GV,Tippett DL,Dusak BA,Paull KD,Plowman J,DeLarco BM,Narayanan VL

    更新日期:1985-11-01 00:00:00

  • Dmp1 physically interacts with p53 and positively regulates p53's stability, nuclear localization, and function.

    abstract::The transcription factor Dmp1 is a Ras/HER2-activated haplo-insufficient tumor suppressor that activates the Arf/p53 pathway of cell-cycle arrest. Recent evidence suggests that Dmp1 may activate p53 independently of Arf in certain cell types. Here, we report findings supporting this concept with the definition of an A...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-11-2410

    authors: Frazier DP,Kendig RD,Kai F,Maglic D,Sugiyama T,Morgan RL,Fry EA,Lagedrost SJ,Sui G,Inoue K

    更新日期:2012-04-01 00:00:00

  • In vitro and in vivo reactivity of an internalizing antibody, RS7, with human breast cancer.

    abstract::RS7, a murine IgG1 antibody raised against human lung carcinoma, possesses pancarcinoma reactivity. The antigen defined by this antibody is present in tumors of the lung, stomach, bladder, breast, ovary, uterus, and prostate. Efficient targeting and therapy by radiolabeled RS7 has been demonstrated previously in anima...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Shih LB,Xuan H,Aninipot R,Stein R,Goldenberg DM

    更新日期:1995-12-01 00:00:00

  • Expression of early growth response genes in human prostate cancer.

    abstract::Early growth-response (EGR) genes are nuclear transcription factors that are implicated in regulating cell proliferation. Because these genes show divergent expression in various human tumors, we sought to determine their expression in nonmalignant and malignant prostate tissues. Total RNA extracted from prostate tiss...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Eid MA,Kumar MV,Iczkowski KA,Bostwick DG,Tindall DJ

    更新日期:1998-06-01 00:00:00

  • Screening prescription drugs for possible carcinogenicity: eleven to fifteen years of follow-up.

    abstract::Using computerized pharmacy records from 1969 to 1973 for a cohort of 143,574 members of the Kaiser Permanente Medical Care Program, we have been testing associations of 215 drugs or drug groups with subsequent incidence of cancer at 56 sites. This paper presents findings with follow-up through 1984. There were 227 st...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Selby JV,Friedman GD,Fireman BH

    更新日期:1989-10-15 00:00:00

  • N,N-Dimethylformamide-induced morphological differentiation and reduction of tumorigenicity in cultured mouse rhabdomyosarcoma cells.

    abstract::N,N-Dimethylformamide treatment of cell cultures established from a transplantable murine rhabdomyosarcoma-induced morphological differentiation and a marked reduction in the tumorigenicity of the sarcoma cells. Fourteen of 17 CE/J mice receiving injections of inducer-treated cells did not develop tumors after 6 month...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Dexter DL

    更新日期:1977-09-01 00:00:00

  • TFAP2C controls hormone response in breast cancer cells through multiple pathways of estrogen signaling.

    abstract::Breast cancers expressing estrogen receptor-alpha (ERalpha) are associated with a favorable biology and are more likely to respond to hormonal therapy. In addition to ERalpha, other pathways of estrogen response have been identified including ERbeta and GPR30, a membrane receptor for estrogen, and the key mechanisms r...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-07-2293

    authors: Woodfield GW,Horan AD,Chen Y,Weigel RJ

    更新日期:2007-09-15 00:00:00

  • In vitro differentiation of teratomas and the distribution of creatine phosphokinase and plasminogen activator in teratocarcinoma-derived cells.

    abstract::Mouse teratocarcinoma cells from embryoid bodies were cultured in vitro to permit their differentiation into a number of cell types. Two enzyme activities, creatine phosphokinase (CPK) and the protease plasminogen activator, were studied to follow the developmental sequence of events in these embryoid body-derived cel...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Topp W,Hall JD,Marsden M,Teresky AK,Rifkin D,Levine AJ,Pollack R

    更新日期:1976-11-01 00:00:00

  • The transcriptional activities of p53 and its homologue p51/p63: similarities and differences.

    abstract::p51/p63 is a novel p53 homologue that has been shown to act as a transcriptional activator through the p53-binding sequence of the p21/WAF1 promoter and to induce apoptosis when it is expressed transiently in a human tumor cell line. We developed transcription assay systems for these two related genes in both Saccharo...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Shimada A,Kato S,Enjo K,Osada M,Ikawa Y,Kohno K,Obinata M,Kanamaru R,Ikawa S,Ishioka C

    更新日期:1999-06-15 00:00:00

  • A cascade of modules of a network defines cancer progression.

    abstract::Similar histologic subtypes of cancers often exhibit different spectrum of genetic and epigenetic alterations. The heterogeneity observed due to lack of consistent and defined alterations affecting a unique set of gene(s) or gene products in cancers derived from a specific tissue, or an organ, pose a challenge in unra...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-06-0993

    authors: Thiagalingam S

    更新日期:2006-08-01 00:00:00

  • Growth phase-dependent expression of ICAD-L/DFF45 modulates the pattern of apoptosis in human colonic cancer cells.

    abstract::The inhibitor of caspase-3-activated DNase (ICAD) is a caspase-3 substrate that controls nuclear apoptosis. ICAD has two isoforms: a functional isoform of M(r) 45,000, ICAD-L/DNA fragmentation factor (DFF) 45; and a M(r) 35,000 isoform, ICAD-S/DFF35. ICAD-deficient murine cells display resistance to apoptotic stimuli ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Charrier L,Jarry A,Toquet C,Bou-Hanna C,Chedorge M,Denis M,Vallette G,Laboisse CL

    更新日期:2002-04-01 00:00:00

  • Intracellular expression of a single-chain antibody directed against human papillomavirus type 16 E7 oncoprotein achieves targeted antineoplastic effects.

    abstract::Human papillomavirus type 16 (HPV16) E7 is a viral oncoprotein that is believed to play a major role in cervical neoplasia. Anti-HPV16 E7 intracellular single-chain antibodies (scFvs) were constructed to down-regulate HPV16 E7 oncoprotein in HPV DNA-containing cell lines. In these studies, we transfected anti-E7 scFvs...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Wang-Johanning F,Gillespie GY,Grim J,Rancourt C,Alvarez RD,Siegal GP,Curiel DT

    更新日期:1998-05-01 00:00:00

  • Predicting response to radioimmunotherapy from the tumor microenvironment of colorectal carcinomas.

    abstract::Solid tumors have a heterogeneous pathophysiology, which directly affects antibody-targeted therapies. Here, we consider the influence of selected tumor parameters on radioimmunotherapy, by comparing the gross biodistribution, microdistribution, and therapeutic efficacy of either radiolabeled or fluorescently labeled ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-07-2967

    authors: El Emir E,Qureshi U,Dearling JL,Boxer GM,Clatworthy I,Folarin AA,Robson MP,Nagl S,Konerding MA,Pedley RB

    更新日期:2007-12-15 00:00:00

  • Mechanism of action of the microtubule-targeted antimitotic depsipeptide tasidotin (formerly ILX651) and its major metabolite tasidotin C-carboxylate.

    abstract::Tasidotin (ILX-651), an orally active synthetic microtubule-targeted derivative of the marine depsipeptide dolastatin-15, is currently undergoing clinical evaluation for cancer treatment. Tasidotin inhibited proliferation of MCF7/GFP breast cancer cells with an IC(50) of 63 nmol/L and inhibited mitosis with an IC(50) ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-06-3065

    authors: Ray A,Okouneva T,Manna T,Miller HP,Schmid S,Arthaud L,Luduena R,Jordan MA,Wilson L

    更新日期:2007-04-15 00:00:00

  • Phosphorylation regulates c-Myc's oncogenic activity in the mammary gland.

    abstract::Expression of the c-Myc oncoprotein is affected by conserved threonine 58 (T58) and serine 62 (S62) phosphorylation sites that help to regulate c-Myc protein stability, and altered ratios of T58 and S62 phosphorylation have been observed in human cancer. Here, we report the development of 3 unique c-myc knock-in mice ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-10-1032

    authors: Wang X,Cunningham M,Zhang X,Tokarz S,Laraway B,Troxell M,Sears RC

    更新日期:2011-02-01 00:00:00

  • Activation of nuclear factor kappaB In vivo selectively protects the murine small intestine against ionizing radiation-induced damage.

    abstract::Exposure of mice to total body irradiation induces nuclear factor kappaB (NFkappaB) activation in a tissue-specific manner. In addition to the spleen, lymph nodes, and bone marrow, the tissues that exhibit NFkappaB activation now include the newly identified site of the intestinal epithelial cells. NFkappaB activated ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-04-0591

    authors: Wang Y,Meng A,Lang H,Brown SA,Konopa JL,Kindy MS,Schmiedt RA,Thompson JS,Zhou D

    更新日期:2004-09-01 00:00:00

  • Chemokine expression in melanoma metastases associated with CD8+ T-cell recruitment.

    abstract::Despite the frequent detection of circulating tumor antigen-specific T cells, either spontaneously or following active immunization or adoptive transfer, immune-mediated cancer regression occurs only in the minority of patients. One theoretical rate-limiting step is whether effector T cells successfully migrate into m...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-08-2281

    authors: Harlin H,Meng Y,Peterson AC,Zha Y,Tretiakova M,Slingluff C,McKee M,Gajewski TF

    更新日期:2009-04-01 00:00:00

  • Temporal patterns of covalent DNA adducts in rat liver after single and multiple doses of aflatoxin B1.

    abstract::We examined patterns of covalent modifications of DNA produced in rat liver after exposure to single and multiple doses of aflatoxin B1. The principal product, previously identified as 2,3-dihydro-3-hydroxy(N7-guanyl) aflatoxin B1, was removed rapidly from liver DNA in vivo after a 0.6-mg/kg dose was administered i.p....

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Croy RG,Wogan GN

    更新日期:1981-01-01 00:00:00

  • Trends in program project grant funding at the National Cancer Institute.

    abstract::In summary, analysis of the P01 program indicates that differences exist in scores and funding requirements between purely basic and translational P01s; P01 funding has been stable and the P01 policies consistent; growth in average costs for P01s has lagged compared to R01s; P01 grantees have a higher success rate tha...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Broder S,Cushing M

    更新日期:1993-02-01 00:00:00

  • Quantitative tumor cytochemistry--G.H.A. Clowes Memorial Lecture.

    abstract::Quantitative optical cytochemistry permits the determination of many different parameters in whole cells or parts of cells. Total amounts of DNA, RNA, and protein and/or the amounts of these substances in nucleus or nucleolus are examples. Techniques in this field have contributed considerably to the development of ou...

    journal_title:Cancer research

    pub_type: 历史文章,杂志文章

    doi:

    authors: Caspersson TO

    更新日期:1979-07-01 00:00:00

  • PDLIM2 Is a Marker of Adhesion and β-Catenin Activity in Triple-Negative Breast Cancer.

    abstract::The PDLIM2 protein regulates stability of transcription factors including NF-κB and STATs in epithelial and hemopoietic cells. PDLIM2 is strongly expressed in certain cancer cell lines that exhibit an epithelial-to-mesenchymal phenotype, and its suppression is sufficient to reverse this phenotype. PDLIM2 supports the ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-18-2787

    authors: Cox OT,Edmunds SJ,Simon-Keller K,Li B,Moran B,Buckley NE,Bustamante-Garrido M,Healy N,O'Flanagan CH,Gallagher WM,Kennedy RD,Bernards R,Caldas C,Chin SF,Marx A,O'Connor R

    更新日期:2019-05-15 00:00:00

  • Differential effects of estrogen and antiestrogen on transforming growth factor gene expression in endometrial adenocarcinoma cells.

    abstract::While antiestrogens are useful agents in the treatment of breast cancer, the usefulness of these agents in the treatment of endometrial cancer remains controversial. There is some concern that the currently available antiestrogens may have partial agonist activity in uterine tissue. To better understand the mechanisms...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Gong Y,Ballejo G,Murphy LC,Murphy LJ

    更新日期:1992-04-01 00:00:00

  • Targeting tumor endothelial marker 8 in the tumor vasculature of colorectal carcinomas in mice.

    abstract::Tumor endothelial marker 8 (TEM8) is a recently described protein that is preferentially expressed within tumor endothelium. We have developed a fusion protein that targets TEM8 and disrupts tumor vasculature by promoting localized thrombosis. Fusion protein specificity and function were evaluated using Western blot a...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-09-0725

    authors: Fernando S,Fletcher BS

    更新日期:2009-06-15 00:00:00

  • Receptors for epidermal growth factor and insulin-like growth factor I and their relation to steroid receptors in human breast cancer.

    abstract::Levels of epidermal growth factor receptor (EGF-R) and insulin-like growth factor receptor (IGF-R) in breast cancer tissue were evaluated. The binding of growth factors was compared to the content of estrogen receptors (ER) and progesterone receptors (PgR). EGF-R correlated negatively to the ER and PgR (Kendall correl...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Pekonen F,Partanen S,Mäkinen T,Rutanen EM

    更新日期:1988-03-01 00:00:00