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  1. 16 Folia Histochemica et Cytobiologica

  2. 3 Acta Biochimica Polonica

  3. 3 Archivum Immunologiae et Therapiae Experimentalis

  4. 1 Cellular and Molecular Biology Letters

  5. 1 Journal of Physiology and Pharmacology

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  1. 4 Krawczyk P.

  2. 4 Naumnik W.

  3. 4 Niklinska W.

  4. 3 Milanowski J.

  5. 3 Wang E.-H.

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  1. 1 2021

  2. 1 2019

  3. 1 2017

  4. 4 2015

  5. 3 2014

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1
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Efficacy of crizotinib therapy for a patient with non-small cell lung cancer with ALK gene rearrangement – case report and review of current therapeutic options

100%
Bargiel J. B., Cabaj J., Chmielewska I., Milanowski J.
Journal of Pre-Clinical and Clinical Research
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2021
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tom 15
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nr 3
2

Reference genes for gene expression studies on non-small cell lung cancer

100%
Gresner P., Gromadzinska J., Wasowicz W.
Acta Biochimica Polonica
|
2009
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tom 56
|
nr 2
307-316
Study Objective: The aim of this study was to test a panel of 6 reference genes in order to identify and validate the most suitable reference genes for expression studies in paired healthy and non-small cell lung cancer tissues. Method: Quantitative real-time PCR followed by the NormFinder- and geNorm-based analysis was employed. The study involved 21 non-small cell lung cancer patients. Results: The analysis of experimental data revealed HPRT1 as the most stable gene followed by RPLP0 and ESD. In contrast, GAPDH was found to be the least stable gene. HPRT1 together with ESD was revealed as the pair of genes introducing the least systematic error into data normalization. Validation by bootstrap random sampling technique and by normalizing exemplary gene expression data confirmed the results. Conclusion: Although HPRT1 and ESD may by recommended for data normalization in gene expression studies on non-small cell lung cancer, the suitability of selected reference genes must be unconditionally validated prior to each study.
3

The presence and clinical implications of alpha-2,6-galactose-linked sialic acids in non-small-cell lung cancer brain metastases - preliminary study

100%
Pelak M. J., Jarosz B., Straczynska-Niemiec A., Krawczyk P., Skoczylas P., Pecka K. M., Snietura M., Szumilo J., Trojanowski T.
Folia Histochemica et Cytobiologica
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2014
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tom 52
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nr 2
4
Content available remote

Evaluation of fluorescence-based methods for total vs. amplifiable DNA quantification in plasma of lung cancer patients

100%
Szpechcinski A., Struniawski R., Zaleska J., Chabowski M., Orlowski T., Roszkowski K., Chorostowska-Wynimko J.
Journal of Physiology and Pharmacology. Supplement
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2008
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tom 59
|
nr 6
675-681
5
Content available remote

The antiproliferative action of [D-Arg1, D-Phe5, D-Trp7,9, Leu11] substance P analogue antagonist against small cell- and non-small-cell lung cancer cells could be due to the pharmacological profile of its tachykinin receptor antagonist

84%
Munoz M., Recio S., Rosso M., Redondo M., Covenas R.
Journal of Physiology and Pharmacology
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2015
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tom 66
|
nr 3
6

Phenotype of dendritic cells generated in the presence of non-small cell lung cancer antigens - preliminary report

84%
Jankowska O., Krawczyk P., Wojas-Krawczyk K., Sagan D., Milanowski J., Rolinski J.
Folia Histochemica et Cytobiologica
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2008
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tom 46
|
nr 4
465-470
7

Prognostic significance of DAPK and RASSF1A promoter hypermethylation in non-small cell lung cancer [NSCLC]

84%
Niklinska W., Naumnik W., Sulewska A., Kozlowski M., Pankiewicz W., Milewski R.
Folia Histochemica et Cytobiologica
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2009
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tom 47
|
nr 2
275-280
8

Immunoexpression of P16INK4a, Rb and TP53 proteins in bronchiolar columnar cell dysplasia [BCCD] in lungs resected due to primary non-small cell lung cancer

84%
Pankiewicz W., Sulewska A., Niklinska W., Naumnik W., Laudanski J., Niklinski J., Chyczewski L.
Folia Histochemica et Cytobiologica
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2008
|
tom 46
|
nr 1
89-96
9

The miR-1204 regulates apoptosis in NSCLC cells by targeting DEK

84%
Qian Z., Yang J., Liu H., Yin Y., Hou L., Hu H.
Folia Histochemica et Cytobiologica
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2019
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tom 57
|
nr 2
10

A quinone-containing compound enhances camptothecin-Induced apoptosis of lung cancer through modulating endogenous ROS and ERK signaling

84%
Chou H.-L., Fong Y., Wei C.-K., Tsai E.-M., Chen J. Y.-F., Chang W.-T., Wu C.-Y., Huang H.-W., Chiu C.-C.
Archivum Immunologiae et Therapiae Experimentalis
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2017
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tom 65
|
nr 3
11

The role of periostin in neoplastic processes

84%
Ratajczak-Wielgomas K., Dziegiel P.
Folia Histochemica et Cytobiologica
|
2015
|
tom 53
|
nr 2
12

CD133-positive cells from non-small cell lung cancer show distinct sensitivity to cisplatin and afatinib

84%
Alama A., Gangemi R., Ferrini S., Barisione G., Orengo A. M., Truini M., Bello M. G. D., Grossi F.
Archivum Immunologiae et Therapiae Experimentalis
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2015
|
tom 63
|
nr 3
13

Differentiation by random amplified polymorphic DNA-polymerase chain reaction (RAPD-PCR) of Candida albicans isolated from upper respiratory tract in patients with non-small cell lung cancer

84%
Biernasiuk A., Korona-Glowniak I., Grzegorczyk A., Malm A.
Acta Biochimica Polonica
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2014
|
tom 61
|
nr 4
14

Association between polymorphisms in CHRNA3 and PHACTR2 gene and environment and NSCLC risk in Chinese population

84%
Lou G., Zhang Y., Bao W., Deng D.
Acta Biochimica Polonica
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2014
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tom 61
|
nr 4
15

The expression of COX-2, hTERT, MDM2, LATS2 and S100A2 in different types of non-small cell lung cancer [NSCLS]

84%
Strazisar M., Mlakar V., Glavac D.
Cellular and Molecular Biology Letters
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2009
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tom 14
|
nr 3
442-456
Several studies have reported different expression levels of certain genes in NSCLC, mostly related to the stage and advancement of the tumours. We investigated 65 stage I-III NSCLC tumours: 32 adenocarcinomas (ADC), 26 squamous cell carcinomas (SCC) and 7 large cell carcinomas (LCC). Using the real-time reverse transcription polymerase chain reaction (RT-PCR), we analysed the expression of the COX-2, hTERT, MDM2, LATS2 and S100A2 genes and researched the relationships between the NSCLC types and the differences in expression levels. The differences in the expression levels of the LATS2, S100A2 and hTERT genes in different types of NSCLC are significant. hTERT and COX-2 were over-expressed and LATS2 under-expressed in all NSCLC. We also detected significant relative differences in the expression of LATS2 and MDM2, hTERT and MDM2 in different types of NSCLC. There was a significant difference in the average expression levels in S100A2 for ADC and SCC. Our study shows differences in the expression patterns within the NSCLC group, which may mimic the expression of the individual NSCLC type, and also new relationships in the expression levels for different NSCLC types.
16

Serum cathepsin K and cystatin C concentration in patients with advanced non-small-cell lung cancer during chemotherapy

84%
Naumnik W., Niklinska W., Ossolinska M., Chyczewska E.
Folia Histochemica et Cytobiologica
|
2009
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tom 47
|
nr 2
207-213
17

The influence of different culture microenvironments on the generation of dendritic cells from non-small-cell lung cancer patients

84%
Krawczyk P., Wojas K., Milanowski J., Rolinski J.
Archivum Immunologiae et Therapiae Experimentalis
|
2007
|
tom 55
|
nr 6
18

Survivin antiapoptotic gene expression as a prognostic factor in non-small cell lung cancer: in situ hybridization study

84%
Karczmarek-Borowska B., Filip A., Wojcierowski J., Smolen A., Pilecka I., Jablonka A.
Folia Histochemica et Cytobiologica
|
2005
|
tom 43
|
nr 4
19

Expression of Fas receptor on peripheral blood lymphocytes from patients with non-small cell lung cancer

84%
Hoser G., Wasilewska D., Domagala-Kulawik J.
Folia Histochemica et Cytobiologica
|
2004
|
tom 42
|
nr 4
20

Connexin 43 recruits E-cadherin expression and inhibits the malignant behaviour of lung cancer cells

67%
Xu H.-T., Li Q.-C., Zhang Y.-X., Zhao Y., Liu Y., Yang Z.-Q., Wang E.-H.
Folia Histochemica et Cytobiologica
|
2008
|
tom 46
|
nr 3
315-321
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