CELL CYCLE PHASES

Tìm thấy 1,908 tài liệu liên quan tới từ khóa "CELL CYCLE PHASES":

PROTEOMIC STUDY REVEALS A FUNCTIONAL NETWORK OF CANCER MARKERS IN THE G1-STAGE OF THE BREAST CANCER CELL CYCLE

PROTEOMIC STUDY REVEALS A FUNCTIONAL NETWORK OF CANCER MARKERS IN THE G1-STAGE OF THE BREAST CANCER CELL CYCLE

Cancer cells are characterized by a deregulated cell cycle that facilitates abnormal proliferation by allowing cells to by-pass tightly regulated molecular checkpoints such as the G1/S restriction point.

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CURCUMIN ANALOG WZ35 INDUCED CELL DEATH VIA ROS-DEPENDENT ER STRESS AND G2/M CELL CYCLE ARREST IN HUMAN PROSTATE CANCER CELLS

CURCUMIN ANALOG WZ35 INDUCED CELL DEATH VIA ROS-DEPENDENT ER STRESS AND G2/M CELL CYCLE ARREST IN HUMAN PROSTATE CANCER CELLS

Prostate cancer is the most commonly diagnosed malignancy among men. The Discovery of new agents for the treatment of prostate cancer is urgently needed. Compound WZ35, a novel analog of the natural product curcumin, exhibited good anti-prostate cancer activity, with an IC50 of 2.2 μM in PC-3 cells.

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SORAFENIB INHIBITS INTRACELLULAR SIGNALING PATHWAYS AND INDUCES CELL CYCLE ARREST AND CELL DEATH IN THYROID CARCINOMA CELLS IRRESPECTIVE OF HISTOLOGICAL ORIGIN OR BRAF MUTATIONAL STATUS

SORAFENIB INHIBITS INTRACELLULAR SIGNALING PATHWAYS AND INDUCES CELL CYCLE ARREST AND CELL DEATH IN THYROID CARCINOMA CELLS IRRESPECTIVE OF HISTOLOGICAL ORIGIN OR BRAF MUTATIONAL STATUS

Patients with dedifferentiated or anaplastic thyroid carcinomas currently lack appropriate treatment options. Kinase inhibitors are among the most promising new agents as alternative strategies. The BRAF- and multi-kinase inhibitor, sorafenib, has already shown antitumor effects in thyroid carcinoma[r]

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HESPERIDIN INHIBITS HELA CELL PROLIFERATION THROUGH APOPTOSIS MEDIATED BY ENDOPLASMIC RETICULUM STRESS PATHWAYS AND CELL CYCLE ARREST

HESPERIDIN INHIBITS HELA CELL PROLIFERATION THROUGH APOPTOSIS MEDIATED BY ENDOPLASMIC RETICULUM STRESS PATHWAYS AND CELL CYCLE ARREST

Hesperidin (30, 5, 9-dihydroxy-40-methoxy-7-orutinosyl flavanone) is a flavanone that is found mainly in citrus fruits and has been shown to have some anti-neoplastic effects. The aim of the present study was to investigate the effect of hesperidin on apoptosis in human cervical cancer HeLa cells an[r]

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EXPRESSION OF MIR-34C INDUCES G2/M CELL CYCLE ARREST IN BREAST CANCER CELLS

EXPRESSION OF MIR-34C INDUCES G2/M CELL CYCLE ARREST IN BREAST CANCER CELLS

MicroRNA-34 is a family of three miRNAs that have been reported to function as tumor suppressor miRNAs and show decreased expression in various cancers. Here, we examine functions of miR-34c in basal-like breast cancer cells.

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DIACEREIN RETARDS CELL GROWTH OF CHONDROSARCOMA CELLS AT THE G2/M CELL CYCLE CHECKPOINT VIA CYCLIN B1/CDK1 AND CDK2 DOWNREGULATION

DIACEREIN RETARDS CELL GROWTH OF CHONDROSARCOMA CELLS AT THE G2/M CELL CYCLE CHECKPOINT VIA CYCLIN B1/CDK1 AND CDK2 DOWNREGULATION

Chondrosarcoma is characterized for its lack of response to conventional cytotoxic chemotherapy, propensity for developing lung metastases, and low rates of survival. Research within the field of development and expansion of new treatment options for unresectable or metastatic diseases is of particu[r]

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RANDOMIZED PHASE II STUDY OF PACLITAXEL/ CARBOPLATIN INTERCALATED WITH GEFITINIB COMPARED TO PACLITAXEL/CARBOPLATIN ALONE FOR CHEMOTHERAPYNAÏVE NON-SMALL CELL LUNG CANCER IN A CLINICALLY

RANDOMIZED PHASE II STUDY OF PACLITAXEL/ CARBOPLATIN INTERCALATED WITH GEFITINIB COMPARED TO PACLITAXEL/CARBOPLATIN ALONE FOR CHEMOTHERAPYNAÏVE NON-SMALL CELL LUNG CANCER IN A CLINICALLY

Considering cell cycle dependent cytotoxicity, intercalation of chemotherapy and epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) may be a treatment option in non-small cell lung cancer (NSCLC).

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PRIMA-1MET INDUCES DEATH IN SOFT-TISSUE SARCOMAS CELL INDEPENDENT OF P53

PRIMA-1MET INDUCES DEATH IN SOFT-TISSUE SARCOMAS CELL INDEPENDENT OF P53

The aim of this study was to explore the efficacy and define mechanisms of action of PRIMA-1MET as a TP53 targeted therapy in soft-tissue sarcoma (STS) cells. Methods: We investigated effects of PRIMA-1MET on apoptosis, cell cycle, and induction of oxidative stress and autophagy in a panel of 6 STS[r]

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ROLE OF SMC1A OVEREXPRESSION AS A PREDICTOR OF POOR PROGNOSIS IN LATE STAGE COLORECTAL CANCER

ROLE OF SMC1A OVEREXPRESSION AS A PREDICTOR OF POOR PROGNOSIS IN LATE STAGE COLORECTAL CANCER

Structural maintenance of chromosomes 1A (SMC1A) is a member of the cohesion family of proteins that plays crucial roles in cell cycle control. Recent studies have concluded that SMC1A is involved in the pathogenesis of cancer.

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RESVERATROL INDUCES AUTOPHAGY-DEPENDENT APOPTOSIS IN HL-60 CELLS

RESVERATROL INDUCES AUTOPHAGY-DEPENDENT APOPTOSIS IN HL-60 CELLS

All known mechanisms of apoptosis induced by resveratrol act through cell cycle arrest and changes in mitochondrial membrane potential. It is currently unknown whether resveratrol-induced apoptosis is associated with other physiological processes, such as autophagy.

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NOVEL SMALL MOLECULE SIRT2 INHIBITORS INDUCE CELL DEATH IN LEUKEMIC CELL LINES

NOVEL SMALL MOLECULE SIRT2 INHIBITORS INDUCE CELL DEATH IN LEUKEMIC CELL LINES

Sirtuin 2 (SIRT2) is a member of the sirtuin family, nicotinamide adenine dinucleotide+ -dependent deacylases, which participates in modulation of cell cycle control, neurodegeneration, and tumorigenesis. SIRT2 expression increases in acute myeloid leukemia blasts.

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COMPARING AMH AFC AND FSH FOR PREDICTING HIGH OVARIAN RESPONSE IN WOMEN UNDERGOING ANTAGONIST PROTOCO1L

COMPARING AMH AFC AND FSH FOR PREDICTING HIGH OVARIAN RESPONSE IN WOMEN UNDERGOING ANTAGONIST PROTOCO1L

mice. In PKCδ null mice, actively dividing cellsare located in basal epithelium and perigemmal edge cells around taste buds, as is thecase in wild type mice. The proliferation indexof the taste epithelium in PKCδ mice is also nophenotype; furthermore, this may suggest thatPKCδ is only activated foll[r]

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PHOSPHORYLATION OF A SPLICE VARIANT OF COLLAPSIN RESPONSE MEDIATOR PROTEIN 2 IN THE NUCLEUS OF TUMOUR CELLS LINKS CYCLIN DEPENDENT KINASE-5 TO ONCOGENESIS

PHOSPHORYLATION OF A SPLICE VARIANT OF COLLAPSIN RESPONSE MEDIATOR PROTEIN 2 IN THE NUCLEUS OF TUMOUR CELLS LINKS CYCLIN DEPENDENT KINASE-5 TO ONCOGENESIS

Cyclin-dependent protein kinase-5 (CDK5) is an unusual member of the CDK family as it is not cell cycle regulated. However many of its substrates have roles in cell growth and oncogenesis, raising the possibility that CDK5 modulation could have therapeutic benefit.

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MICRORNA ALTERATIONS IN ALDH POSITIVE MAMMARY EPITHELIAL CELLS: A CRUCIAL CONTRIBUTING FACTOR TOWARDS BREAST CANCER RISK REDUCTION IN CASE OF EARLY PREGNANCY

MICRORNA ALTERATIONS IN ALDH POSITIVE MAMMARY EPITHELIAL CELLS: A CRUCIAL CONTRIBUTING FACTOR TOWARDS BREAST CANCER RISK REDUCTION IN CASE OF EARLY PREGNANCY

MicroRNAs have recently succeeded in grabbing the center stage in cancer research for their potential to regulate vital cellular process like cell cycle, stem cell renewal and epithelial mesenchymal transition. Breast cancer is the second most leading cause of cancer related mortality in women.

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BOTH TALIN-1 AND TALIN-2 CORRELATE WITH MALIGNANCY POTENTIAL OF THE HUMAN HEPATOCELLULAR CARCINOMA MHCC-97 L CELL

BOTH TALIN-1 AND TALIN-2 CORRELATE WITH MALIGNANCY POTENTIAL OF THE HUMAN HEPATOCELLULAR CARCINOMA MHCC-97 L CELL

Talin-1 (TLN-1) and TLN-2 are implicated in many cellular processes, but their roles in hepatocellular carcinoma (HCC) remain unclear. This study aimed to assess cell cycle distribution, anoikis, invasion and migration in human HCC MHCC-97 L cells.

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MOLECULAR CHARACTERISATION OF ISOGENIC TAXANE RESISTANT CELL LINES IDENTIFY NOVEL DRIVERS OF DRUG RESISTANCE

MOLECULAR CHARACTERISATION OF ISOGENIC TAXANE RESISTANT CELL LINES IDENTIFY NOVEL DRIVERS OF DRUG RESISTANCE

Taxanes such as paclitaxel and docetaxel are used successfully to treat breast cancer, usually in combination with other agents. They interfere with microtubules causing cell cycle arrest; however, the mechanisms underlying the clinical effects of taxanes are yet to be fully elucidated.

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BRCA1 ALTERNATIVE SPLICING LANDSCAPE IN BREAST TISSUE SAMPLES

BRCA1 ALTERNATIVE SPLICING LANDSCAPE IN BREAST TISSUE SAMPLES

BRCA1 is a key protein in cell network, involved in DNA repair pathways and cell cycle. Recently, the ENIGMA consortium has reported a high number of alternative splicing (AS) events at this locus in blood-derived samples.

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CRITICAL ROLE OF CDK11P58 IN HUMAN BREAST CANCER GROWTH AND ANGIOGENESIS

CRITICAL ROLE OF CDK11P58 IN HUMAN BREAST CANCER GROWTH AND ANGIOGENESIS

A capillary network is needed in cancer growth and metastasis. Induction of angiogenesis represents one of the major hallmarks of cancer. CDK11p58, a Ser/Thr kinase that belongs to the Cell Division Cycle 2-like 1 (CDC2L1) subfamily is associated with cell cycle progression, tumorigenesis, sister ch[r]

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POLYPLOID GIANT CANCER CELLS WITH BUDDING AND THE EXPRESSION OF CYCLIN E, S-PHASE KINASE-ASSOCIATED PROTEIN 2, STATHMIN ASSOCIATED WITH THE GRADING AND METASTASIS IN SEROUS OVARIAN TUMOR

POLYPLOID GIANT CANCER CELLS WITH BUDDING AND THE EXPRESSION OF CYCLIN E, S-PHASE KINASE-ASSOCIATED PROTEIN 2, STATHMIN ASSOCIATED WITH THE GRADING AND METASTASIS IN SEROUS OVARIAN TUMOR

We previously reported that polyploid giant cancer cells (PGCCs) exhibit cancer stem cell properties and express cell cycle-related proteins. HEY PGCCs induced by cobalt chloride generated daughter cells and the daughter cells had a strong migratory and invasive ability.

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In vivo dual targeting of the oncogenic Ether-àgo-go-1 potassium channel by calcitriol and astemizole results in enhanced antineoplastic effects in breast tumors

IN VIVO DUAL TARGETING OF THE ONCOGENIC ETHER-ÀGO-GO-1 POTASSIUM CHANNEL BY CALCITRIOL AND ASTEMIZOLE RESULTS IN ENHANCED ANTINEOPLASTIC EFFECTS IN BREAST TUMORS

Breast cancer cell culture
The MBCDF primary breast cancer cell culture was generated from a biopsy obtained from a radical mastec- tomy performed on a patient with an infiltrating ductal carcinoma stage IV. The protocol was approved by the Human Research Ethics Committee from the In[r]

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