Page last updated: 2024-10-20

pteridines and Cancer of Lung

pteridines has been researched along with Cancer of Lung in 26 studies

Research Excerpts

ExcerptRelevanceReference
"This study investigated the feasibility of predicting the neutropenia-related effects of a therapy that combines the investigational drug BI 2536 (inhibitor of Polo-like kinase 1) and pemetrexed, an approved anticancer drug."7.76Prediction of neutropenia-related effects of a new combination therapy with the anticancer drugs BI 2536 (a Plk1 inhibitor) and pemetrexed. ( Döge, C; Freiwald, M; Fritsch, H; Munzert, G; Soto, E; Staab, A; Trocóniz, IF, 2010)
"By using a mouse model of osteosarcoma induced by paratibial injection of cells, we assessed the impact of Smad7 overexpression or SD-208 on tumor growth, tumor microenvironment, bone remodeling, and metastasis development."3.80Overexpression of smad7 blocks primary tumor growth and lung metastasis development in osteosarcoma. ( Amiaud, J; Bougras, G; Chesneau, J; Heymann, D; Heymann, MF; Lamora, A; Le Deley, MC; Leduc, M; Redini, F; Stresing, V; Talbot, J; Taurelle, J; Verrecchia, F, 2014)
"This study investigated the feasibility of predicting the neutropenia-related effects of a therapy that combines the investigational drug BI 2536 (inhibitor of Polo-like kinase 1) and pemetrexed, an approved anticancer drug."3.76Prediction of neutropenia-related effects of a new combination therapy with the anticancer drugs BI 2536 (a Plk1 inhibitor) and pemetrexed. ( Döge, C; Freiwald, M; Fritsch, H; Munzert, G; Soto, E; Staab, A; Trocóniz, IF, 2010)
"Volasertib is a potent, selective, cell cycle kinase inhibitor that induces mitotic arrest and apoptosis by targeting Polo-like kinase."2.80A Randomized, Open-Label Phase II Trial of Volasertib as Monotherapy and in Combination With Standard-Dose Pemetrexed Compared With Pemetrexed Monotherapy in Second-Line Treatment for Non-Small-Cell Lung Cancer. ( Blais, N; Chu, Q; Ellis, PM; Gu, Y; Hirsh, V; Leighl, NB; Liu, D; Pilz, K; Reaume, MN; Sadrolhefazi, B; Wierzbicki, R, 2015)
"BI 2536 is a potent, highly selective inhibitor of polo-like kinase (Plk) 1."2.78A phase I open-label dose-escalation study of intravenous BI 2536 together with pemetrexed in previously treated patients with non-small-cell lung cancer. ( Chu, QS; Ellis, PM; Fritsch, H; Gaschler-Markefski, B; Gyorffy, S; Laurie, SA; Leighl, N; Munzert, G, 2013)
" Grade 4 neutropenia occurred in 37% of patients; common nonhematologic adverse events were fatigue (31%) and nausea (27%)."2.75The efficacy and safety of BI 2536, a novel Plk-1 inhibitor, in patients with stage IIIB/IV non-small cell lung cancer who had relapsed after, or failed, chemotherapy: results from an open-label, randomized phase II clinical trial. ( Frickhofen, N; Fritsch, H; Gaschler-Markefski, B; Hanft, G; Kortsik, C; Munzert, G; Reck, M; Schuler, M; Sebastian, M; von Pawel, J; Waller, CF, 2010)
"The prognosis of small cell lung cancer (SCLC) is poor despite its good initial response to chemotherapy."1.48Polo-like kinase 1 inhibitor BI 6727 induces DNA damage and exerts strong antitumor activity in small cell lung cancer. ( Lu, G; Wang, Y; Wu, L; Xu, L; Yao, Y; Zhou, J, 2018)
" First, BI 6727 has a pharmacokinetic profile favoring sustained exposure of tumor tissues with a high volume of distribution and a long terminal half-life in mice (V(ss) = 7."1.35BI 6727, a Polo-like kinase inhibitor with improved pharmacokinetic profile and broad antitumor activity. ( Adolf, GR; Baum, A; Garin-Chesa, P; Grauert, M; Haslinger, C; Hoffmann, M; Quant, J; Rudolph, D; Steegmaier, M, 2009)

Research

Studies (26)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (3.85)18.2507
2000's3 (11.54)29.6817
2010's19 (73.08)24.3611
2020's3 (11.54)2.80

Authors

AuthorsStudies
Zhou, J2
Yang, Q1
Lu, L1
Tuo, Z1
Shou, Z1
Cheng, J1
Abdulrahman, N2
Siveen, KS1
Joseph, JM1
Osman, A1
Yalcin, HC1
Hasan, A1
Uddin, S1
Mraiche, F2
Park, S1
Kim, TM1
Cho, SY1
Kim, S1
Oh, Y1
Kim, M1
Keam, B1
Kim, DW1
Heo, DS1
Breitenbuecher, F1
von Pawel, J2
Sebastian, M2
Kortsik, C2
Ting, S1
Kasper, S1
Wohlschläger, J1
Worm, K1
Morresi-Hauf, A1
Schad, A1
Westerwick, D1
Wehler, B1
Werner, M1
Munzert, G6
Gaschler-Markefski, B3
Schmid, KW1
Schuler, M2
Yao, D1
Gu, P1
Wang, Y4
Luo, W1
Chi, H1
Ge, J1
Qian, Y1
Wu, L2
Yao, Y1
Lu, G1
Xu, L1
Viswanath, P2
Peng, S3
Singh, R3
Kingsley, C1
Balter, PA1
Johnson, FM4
Van den Bossche, J1
Deben, C1
De Pauw, I1
Lambrechts, H1
Hermans, C1
Deschoolmeester, V1
Jacobs, J1
Specenier, P1
Pauwels, P1
Vermorken, JB1
Peeters, M1
Lardon, F1
Wouters, A1
Sambandam, V1
Shen, L1
Rao, X1
Fang, B1
Wang, J3
Zhou, W1
Liu, X1
Tu, Z1
Zhang, L1
Ku, X1
Bai, F1
Zhao, Z1
Xu, Y1
Ding, K1
Li, H1
Lamora, A1
Talbot, J1
Bougras, G1
Amiaud, J1
Leduc, M1
Chesneau, J1
Taurelle, J1
Stresing, V1
Le Deley, MC1
Heymann, MF1
Heymann, D1
Redini, F1
Verrecchia, F1
Choi, M1
Kim, W1
Cheon, MG1
Lee, CW1
Kim, JE1
Ellis, PM2
Leighl, NB1
Hirsh, V1
Reaume, MN1
Blais, N1
Wierzbicki, R1
Sadrolhefazi, B1
Gu, Y1
Liu, D1
Pilz, K1
Chu, Q1
Ferrarotto, R1
Goonatilake, R2
Yoo, SY1
Tong, P2
Giri, U2
Minna, J1
Girard, L1
Wang, L2
Li, L2
Diao, L1
Peng, DH1
Gibbons, DL1
Glisson, BS1
Heymach, JV2
Byers, LA1
Jaballah, M1
Poomakkoth, N1
Riaz, S1
Abdelaziz, S1
Issa, A1
Nilsson, M1
Villalobos, P1
Mino, B1
Rodriguez-Canales, J1
Wistuba, I1
Kato, T1
Lee, D1
Patel, P1
Young, AJ1
Wada, H1
Hu, HP1
Ujiie, H1
Kaji, M1
Kano, S1
Matsuge, S1
Domen, H1
Kanno, H1
Hatanaka, Y1
Hatanaka, KC1
Kaga, K1
Matsui, Y1
Matsuno, Y1
De Perrot, M1
Yasufuku, K1
Awad, MM1
Chu, QS2
Gandhi, L1
Stephenson, JJ1
Govindan, R1
Bradford, DS1
Bonomi, PD1
Ellison, DM1
Eaton, KD1
Fritsch, H4
Johnson, BE1
Socinski, MA1
Rudolph, D1
Steegmaier, M1
Hoffmann, M1
Grauert, M1
Baum, A1
Quant, J1
Haslinger, C1
Garin-Chesa, P1
Adolf, GR1
Gibbons, SE1
Stayton, I1
Ma, Y1
Reck, M1
Waller, CF1
Frickhofen, N1
Hanft, G1
Soto, E2
Staab, A2
Freiwald, M2
Döge, C1
Trocóniz, IF2
Doege, C1
Leighl, N1
Laurie, SA1
Gyorffy, S1
Ruan, JW1
Huang, JF1
Fu, LW1
Huang, ZS1
Ma, L1
Gu, LQ1
Merz, KH1
Marko, D1
Regiert, T1
Reiss, G1
Frank, W1
Eisenbrand, G1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Randomised Open-label Phase II Trial of BI 6727 Monotherapy and BI 6727 in Combination With Standard Dose Pemetrexed Compared to Pemetrexed Monotherapy in Second Line Non-small Cell Lung Cancer[NCT00824408]Phase 2143 participants (Actual)Interventional2009-03-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

CL of Pemetrexed

CL - total clearance of pemetrexed in plasma after IV administration (NCT00824408)
Timeframe: 5 minutes before pemetrexed infusion, at the end of the infusion and 1.5 hours (h), 2.5h, 4.5h and 25.5h after the end of pemetrexed infusion

InterventionmL/min (Geometric Mean)
Volasertib 250 mg + Pemetrexed 500 mg/m254.4
Volasertib 300 mg + Pemetrexed 500 mg/m269.1

Cmax of Pemetrexed

Cmax - maximum measured concentration of pemetrexed in plasma (NCT00824408)
Timeframe: 5 minutes before pemetrexed infusion, at the end of the infusion and 1.5 hours (h), 2.5h, 4.5h and 25.5h after the end of pemetrexed infusion

Interventionng/mL (Geometric Mean)
Volasertib 250 mg + Pemetrexed 500 mg/m2131000
Volasertib 300 mg + Pemetrexed 500 mg/m2115000

Cmax of Volasertib

Cmax - maximum measured concentration of volasertib in plasma. (NCT00824408)
Timeframe: 5 minutes (min) before the start of Volasertib infusion and 1 hour (h), 2h, 4h, 24h, 168h and 336h after the start of Volasertib infusion

Interventionng/mL (Geometric Mean)
Volasertib 250 mg + Pemetrexed 500 mg/m2554
Volasertib 300 mg + Pemetrexed 500 mg/m2635
Volasertib 300 mg565

Duration of Overall Response

The duration of overall response was measured from the time measurement criteria were met for CR or PR (whichever was first recorded) until the first date that recurrent or progressive disease (PD) was objectively documented (taking as reference for PD the smallest measurements recorded since treatment began). The duration of overall CR was measured from the time measurement criteria were first met for CR until the first date that recurrent disease was objectively documented. Duration of disease control is presented here. (NCT00824408)
Timeframe: From the time measurement criteria were met for CR or PR (whichever was first recorded) until the first date that recurrent or progressive disease was objectively documented

Interventionweeks (Median)
Randomization Phase: Volasertib 300 mg23.0
Randomization Phase: Volasertib 300 mg + Pemetrexed 500 mg/m219.6
Randomization Phase: Pemetrexed 500 mg/m223.4

Occurence of DLT

"Occurence of Dose-limiting toxicity (DLT). A DLT was defined as one or more of the following:~treatment-related CTCAE Grade 3 or 4 nonhematological toxicity (except emesis or diarrhea responding to supportive treatment).~treatment-related CTCAE Grade 4 neutropenia for ≥7 days and/or complicated by infection.~CTCAE Grade 4 thrombocytopenia." (NCT00824408)
Timeframe: Patients were treated for repeated 21-day treatment cycles until disease progression or intolerability of the trial drug, whichever occurred first.

Interventionparticipants (Number)
Run-in Phase: Volasertib 250 mg + Pemetrexed 500 mg/m21
Run-in Phase: Volasertib 300 mg + Pemetrexed 500 mg/m21

Overall Survival (OS)

Overall survival (OS) was defined as the duration of time from randomization to time of death. (NCT00824408)
Timeframe: From randomization until time of death

Interventionmonths (Median)
Randomization Phase: Volasertib 300 mg22.9
Randomization Phase: Volasertib 300 mg + Pemetrexed 500 mg/m217.1
Randomization Phase: Pemetrexed 500 mg/m217.4

Progression Free Survival (PFS) Time From the Date of Randomization to Date of Disease Progression or Death, Whichever Occurred First.

"Disease progression was defined according to the Response Evaluation Criteria in Solid Tumours (RECIST)) criteria. Progression-free survival time was calculated as the duration from the date of randomization to the date of disease progression or death, whichever occured first. For patients with known date of progression (or death): PFS [days] = min (date of progression, date of death) - date of randomization + 1 day. For patients without progression or death, PFS was censored at the last imaging date that showed no disease progression: PFS [days, censored] = date of last imaging showing no progression - date randomization + 1 day.~The number of participants analysed displays the number of patients with an event (progression)." (NCT00824408)
Timeframe: From randomization until disease progression or death

Interventionmonths (Median)
Randomization Phase: Volasertib 300 mg1.4
Randomization Phase: Volasertib 300 mg + Pemetrexed 500 mg/m23.3
Randomization Phase: Pemetrexed 500 mg/m25.3

Total Clearance (CL) of Volasertib

CL - total clearance of volasertib in plasma after IV administration (NCT00824408)
Timeframe: 5 minutes (min) before the start of Volasertib infusion and 1 hour (h), 2h, 4h, 24h, 168h and 336h after the start of Volasertib infusion

InterventionmL/min (Geometric Mean)
Volasertib 250 mg + Pemetrexed 500 mg/m2782
Volasertib 300 mg + Pemetrexed 500 mg/m2882
Volasertib 300 mg867

Vss of Pemetrexed

Vss - apparent volume of distribution at steady state following IV administration of pemetrexed (NCT00824408)
Timeframe: 5 minutes before pemetrexed infusion, at the end of the infusion and 1.5 hours (h), 2.5h, 4.5h and 25.5h after the end of pemetrexed infusion

InterventionLitres (Geometric Mean)
Volasertib 250 mg + Pemetrexed 500 mg/m29.40
Volasertib 300 mg + Pemetrexed 500 mg/m213.1

Vss of Volasertib

Vss - apparent volume of distribution at steady state following IV administration of volasertib (NCT00824408)
Timeframe: 5 minutes (min) before the start of Volasertib infusion and 1 hour (h), 2h, 4h, 24h, 168h and 336h after the start of Volasertib infusion

InterventionLitres (Geometric Mean)
Volasertib 250 mg + Pemetrexed 500 mg/m26730
Volasertib 300 mg + Pemetrexed 500 mg/m26750
Volasertib 300 mg6230

Frequency of Patients With Possible Clinically Significant Abnormalities

Frequency of patients with possible clinically significant abnormalities (NCT00824408)
Timeframe: From first drug infusion until 21 days after last drug infusion, up to 1100 days

,,,,
Interventionparticipants (Number)
Haemoglobin - LowWhite blood cell ct. - LowWhite blood cell ct. - HighPlatelets - LowPlatelets - HighNeutrophils - LowLymphocytes - LowAST/GOT, SGOT - HighALT/GPT, SGPT - HighAlkaline phosphatase - HighCreatinine - HighBilirubin, total - High
Randomization Phase: Pemetrexed 500 mg/m21412123122236501
Randomization Phase: Volasertib 300 mg1615183131600001
Randomization Phase: Volasertib 300 mg + Pemetrexed 500 mg/m221250302322610031
Run-in Phase: Volasertib 250 mg + Pemetrexed 500 mg/m2140004400001
Run-in Phase: Volasertib 300 mg + Pemetrexed 500 mg/m2220112411000

Objective Tumor Response, Defined as Complete Response (CR), and Partial Response (PR), Evaluated According to RECIST Criteria.

Objective tumor response, defined as complete response (CR), and partial response (PR), evaluated according to RECIST criteria. Evaluation of target lesions: Complete Response (CR): disappearance of all target lesions. Partial Response (PR): ≥30% decrease in the sum of the longest diameter of target lesions, taking as reference the baseline sum longest diameter. Evaluation of nontarget lesions: Complete Response (CR): disappearance of all nontarget lesions. (NCT00824408)
Timeframe: From first drug infusion until 21 days after last drug infusion, up to 1100 days

,,,,
Interventionpercentage of participants (Number)
Complete response (CR)Partial response (PR)
Randomization Phase: Pemetrexed 500 mg/m20.010.6
Randomization Phase: Volasertib 300 mg0.08.1
Randomization Phase: Volasertib 300 mg + Pemetrexed 500 mg/m20.021.3
Run-in Phase: Volasertib 250 mg + Pemetrexed 500 mg/m20.016.7
Run-in Phase: Volasertib 300 mg + Pemetrexed 500 mg/m20.050.0

Occurrence and Intensity of AEs Graded According to CTCAE.

All patients were carefully monitored during and after each treatment cycle. Adverse events (AEs) were recorded and were graded according to the National Cancer Institute - Common Terminology Criteria for Adverse Events (CTCAE). (NCT00824408)
Timeframe: From first drug infusion until 21 days after last drug infusion, up to 1100 days

,,,,
Interventionparticipants (Number)
CTCAE Grade 1CTCAE Grade 2CTCAE Grade 3CTCAE Grade 4CTCAE Grade 5
Randomization Phase: Pemetrexed 500 mg/m26181550
Randomization Phase: Volasertib 300 mg612863
Randomization Phase: Volasertib 300 mg + Pemetrexed 500 mg/m22181952
Run-in Phase: Volasertib 250 mg + Pemetrexed 500 mg/m200330
Run-in Phase: Volasertib 300 mg + Pemetrexed 500 mg/m202310

Trials

6 trials available for pteridines and Cancer of Lung

ArticleYear
Comprehensive Biomarker Analyses in Patients with Advanced or Metastatic Non-Small Cell Lung Cancer Prospectively Treated with the Polo-Like Kinase 1 Inhibitor BI2536.
    Oncology research and treatment, 2017, Volume: 40, Issue:7-8

    Topics: Antimitotic Agents; Biomarkers, Tumor; Carcinoma, Non-Small-Cell Lung; Cohort Studies; Disease Progr

2017
A Randomized, Open-Label Phase II Trial of Volasertib as Monotherapy and in Combination With Standard-Dose Pemetrexed Compared With Pemetrexed Monotherapy in Second-Line Treatment for Non-Small-Cell Lung Cancer.
    Clinical lung cancer, 2015, Volume: 16, Issue:6

    Topics: Adult; Aged; Aged, 80 and over; Carcinoma, Non-Small-Cell Lung; Cell Cycle Proteins; Drug Dosage Cal

2015
An open-label, phase II study of the polo-like kinase-1 (Plk-1) inhibitor, BI 2536, in patients with relapsed small cell lung cancer (SCLC).
    Lung cancer (Amsterdam, Netherlands), 2017, Volume: 104

    Topics: Administration, Intravenous; Adult; Aged; Cell Cycle Proteins; Disease-Free Survival; Female; Humans

2017
The efficacy and safety of BI 2536, a novel Plk-1 inhibitor, in patients with stage IIIB/IV non-small cell lung cancer who had relapsed after, or failed, chemotherapy: results from an open-label, randomized phase II clinical trial.
    Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2010, Volume: 5, Issue:7

    Topics: Adenocarcinoma; Adult; Aged; Aged, 80 and over; Carcinoma, Non-Small-Cell Lung; Cell Cycle Proteins;

2010
Comparison of different semi-mechanistic models for chemotherapy-related neutropenia: application to BI 2536 a Plk-1 inhibitor.
    Cancer chemotherapy and pharmacology, 2011, Volume: 68, Issue:6

    Topics: Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Cell Cycle Proteins; Humans; Lung Neoplasms;

2011
A phase I open-label dose-escalation study of intravenous BI 2536 together with pemetrexed in previously treated patients with non-small-cell lung cancer.
    Clinical lung cancer, 2013, Volume: 14, Issue:1

    Topics: Administration, Intravenous; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Carcinoma,

2013

Other Studies

20 other studies available for pteridines and Cancer of Lung

ArticleYear
PLK1 Inhibition Induces Immunogenic Cell Death and Enhances Immunity against NSCLC.
    International journal of medical sciences, 2021, Volume: 18, Issue:15

    Topics: Animals; Carcinoma, Non-Small-Cell Lung; Cell Cycle Proteins; Cell Line, Tumor; Humans; Immunogenic

2021
Inhibition of p90 ribosomal S6 kinase potentiates cisplatin activity in A549 human lung adenocarcinoma cells.
    The Journal of pharmacy and pharmacology, 2020, Volume: 72, Issue:11

    Topics: A549 Cells; Adenocarcinoma of Lung; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Autop

2020
Combined blockade of polo-like kinase and pan-RAF is effective against NRAS-mutant non-small cell lung cancer cells.
    Cancer letters, 2020, 12-28, Volume: 495

    Topics: Aged; Carcinoma, Non-Small-Cell Lung; Cell Cycle Proteins; Cell Line, Tumor; Cell Proliferation; Cel

2020
Inhibiting polo-like kinase 1 enhances radiosensitization via modulating DNA repair proteins in non-small-cell lung cancer.
    Biochemistry and cell biology = Biochimie et biologie cellulaire, 2018, Volume: 96, Issue:3

    Topics: Apoptosis; Carcinoma, Non-Small-Cell Lung; Cell Cycle Proteins; Cell Line, Tumor; Chromosome Segrega

2018
Polo-like kinase 1 inhibitor BI 6727 induces DNA damage and exerts strong antitumor activity in small cell lung cancer.
    Cancer letters, 2018, 11-01, Volume: 436

    Topics: Animals; Apoptosis; Cell Cycle Proteins; Cell Line, Tumor; Cell Proliferation; DNA Damage; Female; G

2018
A Novel Method for Quantifying Total Thoracic Tumor Burden in Mice.
    Neoplasia (New York, N.Y.), 2018, Volume: 20, Issue:10

    Topics: Animals; Antineoplastic Agents; Lung Neoplasms; Male; Mice, Inbred Strains; Mice, Transgenic; Neopla

2018
In vitro study of the Polo-like kinase 1 inhibitor volasertib in non-small-cell lung cancer reveals a role for the tumor suppressor p53.
    Molecular oncology, 2019, Volume: 13, Issue:5

    Topics: A549 Cells; Apoptosis; Biomarkers, Tumor; Carcinoma, Non-Small-Cell Lung; Cell Cycle Proteins; Cell

2019
Non-canonical cMet regulation by vimentin mediates Plk1 inhibitor-induced apoptosis.
    EMBO molecular medicine, 2019, Volume: 11, Issue:5

    Topics: Animals; Apoptosis; Carcinoma, Non-Small-Cell Lung; Cell Cycle Proteins; Cell Line, Tumor; Drug Resi

2019
Discovery of pteridin-7(8H)-one-based irreversible inhibitors targeting the epidermal growth factor receptor (EGFR) kinase T790M/L858R mutant.
    Journal of medicinal chemistry, 2013, Oct-24, Volume: 56, Issue:20

    Topics: Animals; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Cell Proliferation; Computational Biology

2013
Overexpression of smad7 blocks primary tumor growth and lung metastasis development in osteosarcoma.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2014, Oct-01, Volume: 20, Issue:19

    Topics: Animals; Bone Neoplasms; Bone Resorption; Cell Line, Tumor; Disease Models, Animal; Female; Gene Exp

2014
Polo-like kinase 1 inhibitor BI2536 causes mitotic catastrophe following activation of the spindle assembly checkpoint in non-small cell lung cancer cells.
    Cancer letters, 2015, Feb-28, Volume: 357, Issue:2

    Topics: Antimitotic Agents; Apoptosis; Blotting, Western; Carcinoma, Non-Small-Cell Lung; Cell Cycle Protein

2015
Epithelial-Mesenchymal Transition Predicts Polo-Like Kinase 1 Inhibitor-Mediated Apoptosis in Non-Small Cell Lung Cancer.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2016, Apr-01, Volume: 22, Issue:7

    Topics: Animals; Apoptosis; Benzimidazoles; Carcinoma, Non-Small-Cell Lung; Cell Cycle Checkpoints; Cell Cyc

2016
Inhibition of p90 ribosomal S6 kinase attenuates cell migration and proliferation of the human lung adenocarcinoma through phospho-GSK-3β and osteopontin.
    Molecular and cellular biochemistry, 2016, Volume: 418, Issue:1-2

    Topics: Adenocarcinoma; Cell Movement; Cell Proliferation; Gene Expression Regulation, Neoplastic; Glycogen

2016
Polo-like kinase 1 inhibition diminishes acquired resistance to epidermal growth factor receptor inhibition in non-small cell lung cancer with T790M mutations.
    Oncotarget, 2016, Jul-26, Volume: 7, Issue:30

    Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Carcinoma, Non-Small-Cell Lung; Cell Cycle

2016
SORORIN and PLK1 as potential therapeutic targets in malignant pleural mesothelioma.
    International journal of oncology, 2016, Volume: 49, Issue:6

    Topics: Adaptor Proteins, Signal Transducing; Adult; Aged; Aged, 80 and over; Biomarkers, Tumor; Cell Cycle

2016
BI 6727, a Polo-like kinase inhibitor with improved pharmacokinetic profile and broad antitumor activity.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2009, May-01, Volume: 15, Issue:9

    Topics: Animals; Antineoplastic Agents; Apoptosis; Blotting, Western; Carcinoma, Non-Small-Cell Lung; Cell C

2009
Optimization of urinary pteridine analysis conditions by CE-LIF for clinical use in early cancer detection.
    Electrophoresis, 2009, Volume: 30, Issue:20

    Topics: Drug Stability; Early Detection of Cancer; Electrophoresis, Capillary; Humans; Lung Neoplasms; Pteri

2009
Prediction of neutropenia-related effects of a new combination therapy with the anticancer drugs BI 2536 (a Plk1 inhibitor) and pemetrexed.
    Clinical pharmacology and therapeutics, 2010, Volume: 88, Issue:5

    Topics: Antimetabolites, Antineoplastic; Antineoplastic Combined Chemotherapy Protocols; Carcinoma, Non-Smal

2010
[Synthesis and antitumour activities of some pteridine derivatives].
    Yao xue xue bao = Acta pharmaceutica Sinica, 2004, Volume: 39, Issue:5

    Topics: Adenocarcinoma; Antineoplastic Agents; Cell Line, Tumor; Humans; KB Cells; Lung Neoplasms; Molecular

2004
Synthesis of 7-benzylamino-6-chloro-2-piperazino-4-pyrrolidinopteridine and novel derivatives free of positional isomers. Potent inhibitors of cAMP-specific phosphodiesterase and of malignant tumor cell growth.
    Journal of medicinal chemistry, 1998, Nov-19, Volume: 41, Issue:24

    Topics: 3',5'-Cyclic-AMP Phosphodiesterases; Animals; Antineoplastic Agents; Cell Division; Crystallography,

1998