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001 | 648492 | ||
005 | 20231030040838.0 | ||
035 | _a(RuTPU)RU\TPU\network\13651 | ||
090 | _a648492 | ||
100 | _a20160523a2016 k y0engy50 ba | ||
101 | 0 | _aeng | |
135 | _adrcn ---uucaa | ||
181 | 0 | _ai | |
182 | 0 | _ab | |
200 | 1 |
_aRecurrence of squamous cell lung carcinoma is associated with the co-presence of reactive lesions in tumor-adjacent bronchial epithelium _fO. V. Pankova [et al.] |
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203 |
_aText _celectronic |
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300 | _aTitle screen | ||
320 | _a[References: 35 tit.] | ||
330 | _aRecurrences occur in 30 % of lung cancer patients after radical therapy; however, known prognostic factors are not always effective. In this study, we investigated whether the frequency of squamous non-small cell lung cancer (NSCLC) recurrence depends on the presence of reactive lesions in tumor-adjacent bronchial epithelium. Specimens of adjacent lung tissue from 104 patients with squamous NSCLC were used for the determination of basal cell hyperplasia (BCH) and squamous metaplasia (SM) and for the analysis of the expression of Ki-67, p53, Bcl-2, and CD138. We found that recurrence was observed in 36.7 % of patients with BCH combined with SM (BCH + SM+) in the same bronchus, compared with 1.8 % in patients with isolated BCH (BCH + SM?; odds ratio (OR) 31.26, 95 % confidence interval (CI) 3.77–258.60; p=?0.00002). The percentage of Ki-67-positive cells was significantly higher in BCH + SM+ than in BCH + SM? (34.9 vs. 18.3 %; effect size 2.86, 95 % CI 2.23–3.47; p?=?0.003). P53 expression was also more significant in BCH + SM+ than in BCH + SM? (14.4 vs. 9.6 %; effect size 1.22, 95 % CI 0.69–1.76; p=0.0008). In contrast, CD138 expression was lower in BCH + SM+ than in BCH + SM (21.8 vs. 38.5 %; effect size ?6.26, 95 % CI ?7.31 to ?5.22; p=?0.003). Based on our results, we concluded that the co-presence of reactive bronchial lesions is associated with the development of recurrent squamous NSCLC and may be a negative prognostic indicator. In addition, significant differences in Ki-67, p53, and CD138 expression exist between isolated BCH and BCH combined with SM that probably reflect part of biological differences, which could relate to the mechanism of lung cancer recurrence. | ||
333 | _aРежим доступа: по договору с организацией-держателем ресурса | ||
461 |
_tTumor Biology _oScientific Journal _d1965- |
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463 |
_tVol. 37, iss. 3 _v[P. 3599-3609] _d2016 |
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610 | 1 | _aэлектронный ресурс | |
610 | 1 | _aтруды учёных ТПУ | |
610 | 1 | _aрекуррентность | |
610 | 1 | _aрак легких | |
701 | 1 |
_aPankova _bO. V. _gOlga Vladimirovna |
|
701 | 1 |
_aDenisov _bE. V. _gEvgeny Vladimirovich |
|
701 | 1 |
_aPonomareva _bA. A. _cbiologist _cexpert of Tomsk Polytechnic University, candidate of biological sciences _f1985- _gAnastasiya Alekseevna _2stltpush _3(RuTPU)RU\TPU\pers\36792 |
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701 | 1 |
_aGerashchenko _bT. S. _gTatiana Sergeevna |
|
701 | 1 |
_aTuzikov _bS. A. _gSergey Alexandrovich |
|
701 | 1 |
_aPerelmuter _bV. M. _gVladimir Mikhaylovich |
|
712 | 0 | 2 |
_aНациональный исследовательский Томский политехнический университет (ТПУ) _bФизико-технический институт (ФТИ) _bКафедра прикладной физики (№ 12) (ПФ) _h46 _2stltpush _3(RuTPU)RU\TPU\col\18729 |
801 | 2 |
_aRU _b63413507 _c20160524 _gRCR |
|
856 | 4 | 0 | _uhttp://dx.doi.org/10.1007/s13277-015-4196-2 |
942 | _cCF |