Micropapillary: A component more likely to harbour heterogeneous EGFR mutations in lung adenocarcinomas


The micropapillary (MP) subtype has recently been established to be a distinct marker of poor prognosis in lung adenocarcinomas (LACs). According to the 2015 WHO classification system, LAC constituents are required to be precisely reported. T790M mutation and an insertion in exon 20 (E20ins) are associated with EGFR-TKI resistance. A total of 211 LAC patients were involved in this study, and EGFR mutations were determined using an amplification refractory mutation system (ARMS). Sex, smoking history, lymph node status, and clinical stage differed significantly between the EGFR wild type and mutant groups (p < 0.05). The EGFR mutation occurred more frequently in female, non-smokers, ACs with papillary (85.7%) or MP components (91.4%) (p < 0.001). Twenty ACs with naïve T790M or E20ins were microdissected. The AC constituents metastasizing to lymph nodes exhibited a phenotype and EGFR status that was consistent with the primary loci constituents. Glomerulus-like solid components exhibited the same EGFR status as the surrounding T790M-mutated MP components. The MP and glomerulus-like portions in AC tumours exhibited a congenial EGFR status, but the acinar cells with papillary cells were heterogeneous. The naïve T790M mutants, although minor in the MP component, dramatically increased after EGFR-TKI therapy and indicate that the MP components feature intrinsic heterogeneity.


Adenocarcinoma (AC) is one of the most common histological types of non-small cell lung cancer (NSCLC)1. More than 80% of lung ACs are diagnosed based on tumour constituent mixtures in accordance with the 2004 WHO classification system. New classification systems that better considered the proportions of AC components were then established by the International Association for the Study of Lung Cancer (IASL), the American Thoracic Society (ATS) and the European Respiratory Society (ERS) in 20112, as well as the WHO classification system in 20153. These new classification systems aim to classify invasive adenocarcinoma histological subtypes according to their precise components, such as lepidic (formerly the most mixed tumour subtype with nonmucinous BAC), mucinous (formerly mucinous BAC), acinar, papillary, solid patterns and micropapillary (MP) ACs. These systems have demonstrated an improved ability to address complex histological phenotypes and improve molecular and prognostic correlations4. Recent studies of stage IB lung ACs report that micropapillary ACs are predominant and are the most common AC subtype with an EGFR mutation, whereas predominantly solid ACs present with a lower frequency5. Specifically, the MP subtype is associated with worse outcomes6,7. Notably, several recent studies have noted that the MP pattern may have a clinical impact on patient survival rates8,9. According to the new WHO classification system, all components in the bulk of a tumour are required to be listed in precise proportions. In another study, 20 out of 21 (95.2%) MP-predominant lung adenocarcinomas harboured EGFR (85.7%) driver mutations. MP-predominant ACs are more likely to recur than ACs harbouring MP components (>5%) in stage I lung AC10.

EGFR mutations occurring between exon 18 and exon 21 are associated with a response to tyrosine kinase inhibitors (TKIs), and EGFR mutations are mainly categorized as activating (frame deletion in exon 19 and L858R) or TKI-resistant (T790M and insertions in exon 20) mutations11,12,13. The T790M mutation was initially considered to be a secondary mutation following progression after EGFR-TKI therapy, but several recent reports have suggested that T790M exists at a low frequency before EGFR-TKI therapy14,15. Moreover, using highly sensitive methods, studies have shown that T790M frequencies range from 40% to 79%, even in EGFR-TKI-naïve NSCLC patients harbouring EGFR-sensitive mutations16,17,18. These results suggest that EGFR-mutated tumours may intrinsically include a minor population of T790M-positive cancer cells. At an advanced stage, lung cancers are inoperable, and targeted therapy is critical for such patients. Therefore, the main issue for modern biomedical research is understanding cellular and molecular mechanisms. Because the association between morphological diversity and biological heterogeneity in ‘mixed’ ACs remains unclear, understanding the relationship between histological and biological attributes in AC components is critical. In our previous study, we used a high-resolution melt (HRM) curve to screen EGFR statuses in AC primary and metastasized tumours and found different EGFR statuses among these tumours (Fig. 1). Because laser capture microdissection (LCM) enables researchers to combine structural identification with molecular investigation, these methods aid in investigating pathological changes on a molecular, cellular, or tissue level19. The purpose of the current study is to analyse the correlation between de novo EGFR-TKI-resistant mutations and histological diversity in AC subtypes.

Figure 1: Exon 19 status of the EGFR gene was screened using high-resolution melting curves in the primary and metastasized tumours of a ‘mixed’ AC.

The ‘mixed’ AC was composed of micropapillary (black arrow) and acinar (red arrow) patterns in the primary locus (a, ×200), whereas only acinar cells occupied the metastasized lymph node and destroyed its normal structure (b, ×40). An HRM analysis of the EGFR status shows that the primary lesion curve (black arrow) exhibited a different character compared with a metastasized tumour (green arrow) and peripheral normal tissue (blue arrow)(c).


Patient Characteristics and Histopathological Features

Clinicopathological features are summarized in Table 1. A total of 211 patients with invasive AC were observed; invasive AC was slightly more common in females (51.7%, n = 109) than in males. The median age was 61 years for the females (range, 34–87 years) and 60 years for the males (range, 33–82 years). Of the 211 patients, 142 (67.3%) had never smoke. Eighty-eight cases (41.7%) were stage I or II; 84 (39.8%) were stage IIIA; and 39 (18.5%) were stage IIIB or IV. Fifty-eight (27.5%) and 98 (46.4%) ACs featured MP or papillary patterns, respectively. Furthermore, 29.8% of the cases were diagnosed of as pure papillary AC, and 11.8% cases were diagnosed as pure MP AC. Of the 135 ACs with local lymph node invasion, 74.1% (43/58) of tumours harbouring an MP pattern exhibited more aggressive growth (p = 0.04, one sided comparison). The other ACs contained solid, acinar, lepidic or mucinous components. We analysed the primary ACs and metastasized AC phenotypes (Fig. 1), and the metastasized neoplastic cells featured one or more of the patterns in the primary loci.

Table 1 Clinicopathological characteristics and EGFR status in 211 AC patients.

Histological Subtypes and EGFR Mutation Analysis

Of the 211 AC tumours, 117 (55.5%) featured an EGFR-sensitive mutation (deletion in the exon 19 frame, or L858R), and 67 were EGFR wild typed. The T790M and insertion mutations in exon 20 (E20ins) were the EGFR-TKI-resistant mutations identified in our study. Twenty ACs (9.5%) featured a de novo EGFR-TKI-resistant mutation, either with a sensitive mutation (7.1%) or independently (2.3%). Six ACs (2.8%) featured less frequent mutations, such as G719X, L861Q and S768I. Only one AC included both a frame deletion in exon 19 (E19del) and L858R. The presence of EGFR mutations significantly correlated with gender and smoking status, especially in females (78.9%, p < 0.001), non-smokers (76.8%, p < 0.001) and histological subtypes with MP (91.4%, p < 0.001) and papillary components (83.7%, p < 0.001). Ninety percent of the 30 ACs with both papillary and MP components as the predominant components included an EGFR mutation. Similarly, ACs with a predominant pattern with either papillary or MP components also exhibited a higher EGFR mutation incidence (83.3% and 92.3%, respectively) than ACs with acinar (60.6%) and lepidic (20%) components. Local lymph nodes were invaded in 135 (64%) ACs. Ninety-seven (68.3%) ACs with an EGFR mutation and 43 (74.1%) ACs with a MP pattern were susceptible to lymph node invasion (p = 0.04, p = 0.04, respectively).

Naïve EGFR-resistant mutations in AC components in both primary and metastasized tumours determined using a HRM curve and ARMS

Twenty ACs with naïve EGFR-TKI resistance were investigated to analyse molecular heterogeneity and phenotype. The specific histological components from the primary and metastasized foci are listed in Table 2. In this study, the sensitive mutations were more likely to accompany the T790M mutation. Eighty-five percent (17/20) of the tumours exhibited papillary or MP architecture. Furthermore, ACs harbouring MP (30%) and papillary (76.9%; 10/13) components were observed with the T790M mutation. In addition, E20ins was detected in 5 ACs, 4 of which were mixed ACs and only one was a pure papillary AC. The acinar pattern was predisposed to E20ins (60%; 3/5). Four ACs were investigated with solid, acinar or lepidic structures and E20ins. Seventeen ACs (85%) were mixed with more than one pattern, and the sensitive and resistant mutation curve cycle threshold (Ct) values differed (Fig. 2). Therefore, we used LMD to discern different morphological tissues and to investigate the EGFR status of the heterogeneous components. The ARMS amplification curves show that the T790M mutation was prevalent in papillary (76.9%; 10/13) and MP (100%; 6/6) components with or without a sensitive mutation (Fig. 2a,b). The discrepant Ct values for each component show that the papillary or MP components exhibited intrinsic heterogeneity (Fig. 2c,d). Furthermore, 53.8% (7/13) of the metastasized tumours exhibited one or more phenotypes of the primary loci (Table 2). An ARMS amplification revealed that the EGFR status of the metastasized cells was consistent with the corresponding primary tumour components.

Table 2 Histological components and naïve EGFR-TKI resistant mutations in primary and metastasized tumours.
Figure 2: Different histological portions of an adenocarcinoma consisting of micropapillary and solid components (patient No 154) were laser microdissected, and EGFR mutants were determined using ARMS.

In the micropapillary portion, small clusters of glandular cells lacking fibrovascular cores grow within an airspace covered by cancer cells (a) and the EGFR status of the tumour mass was demonstrated using L858R (yellow curve) and T790M (green curve) mutations (b). Micropapillary cells were separated by laser microdissection (c), and L858R and T790M were found together (d). In the solid area, malignant cells are woven in tufts as a glomerulus-like pattern (red arrow), and the tumour cells are crowded in a solid or plate structure (e) and were captured using LMD (f). The EGFR mutation status was the same as that of the micropapillary cells (g).

Solid or plate patterns exhibited varied EGFR statuses in different tumour masses. The solid structure coexisted with MP, papillary or even acinar components. A solid structure with papillary or MP components was often accompanied by architectures such as ‘glomerulus’ spreading and transforming to adjacent MP or papillary patterns. The glomerulus-like cell tufts featured both the same cytological features and EGFR status, which indicates that these tufts are woven micropapillae or papillae with a fissure around a lumen (Fig. 2e–g). Furthermore, papillary cells accompanied by MP cells in the bulk of the tumour exhibited the same cytological characteristics. The histological arrangements showed cuboidal or columnar cells growing on a fibrovascular core with an apical cytoplasm protruding into the airspace, similar to a ‘hobnail’. This form was conspicuous and unusual with a conventional papillary pattern (Fig. 3a–c). Acinar cells with papillary cells did not exhibit the same shape as the papillary cells, and molecular heterogeneity was observed when these tumour cells were mixed in a tumour mass (Fig. 3d–f).

Figure 3: An adenocarcinoma composed of papillary and acinar components (patient No. 144) was laser microdissected, and the EGFR mutations were investigated in different histological components.

Cuboidal to columnar cells grow in a layer along fibrovascular cores with papillary pattern. (a) Tumour cells were captured (b) and we determined their composite L858R (yellow curve) and T790M (green curve) mutations (c). Acinar cells did not exhibit the same shape as papillary cells but a glandular pattern (d). Laser-captured cells (e) also featured a wild-type EGFR status, which differed from the papillary cells (f).

In the current study, one MP AC patient progressed to an advanced stage with metastasis to bilateral lung, invasion to parietal layer of pleura and right supraclavicular lymph nodes (T4N3M1a) (Fig. 4a) and then received a needle aspiration on the primary locus. The histological type was MP (Fig. 4b), and the EGFR mutation test using ARMS showed an E19del mutation despite a minute quantity of T790M (for the manual criteria, a positive T790M requires that the Ct value is ≤28 cycles) (Fig. 4c). Tumour size obviously shrank after 9 months Iressa therapy (Fig. 4d). However, the tumour began to progress again (Fig. 4e), and one more biopsy was performed. The tumour histological pattern persisted on the MP components, the newly progressed tumour exhibited poor differentiation (Fig. 4f), and the T790M mutation clearly increased with the E19del (Fig. 4g). This case exhibits the innate heterogeneity of MP ACs.

Figure 4: A patient was used as an example to clarify the heterogeneity of the micropapillary AC.

A tumour mass was present in the inferior lobe of the right lung, which was determined using computed tomography (a) and the histological type was a pure micropapillary type (b). An ARMS analysis of the EGFR status showed a deletion in exon 19 (red curve) and a minor naïve T790M mutation (green curve) (c). Conspicuous inhibition was observed using computer tomography after 9 months of EGFR TKI therapy (d). However, progression of the tumour was observed after 11 months of therapy (e) one more biopsy was performed, and the histological type remained the micropapillary type but with poorer differentiation (f). The T790M mutant had clearly increased in the micropapillary tissue (green curve) (g).


Increasing evidence shows that histological subtype is a prognostic factor that is independent of EGFR mutations20. Articles on the topic of MP ACs have reported patients with a poor prognosis, even at an early stage21,22. A recent study demonstrated that the MP pattern ratio correlated with the TNM stage and lymph node metastasis. Moreover, MP predominant subtypes are more likely to occur with EGFR-mut tumours in Chinese lung AC patients23. Our results also show that EGFR mutation incidence is more frequent in ACs with MP (91.4%) and papillary cells (85.7%), and ACs with EGFR mutations prone to local lymph nodes were observed for the MP components. The MP and solid subtypes are common in tumours past stage I, sizes >2.5 cm and with a pure solid type, which are predictors of poor DFS. The MP subtype is a single prognostic factor for OS9. In this study, MP, papillary and a glomerulus-like solid structure coexisted, and neoplastic cells with a solid area grew in tufts without a fibrovascular core and were crowded in a lumen. In addition, the cells appear as MP cells. The same EGFR status in the MP and solid portions of a tumour mass suggested that they may have the same origin and response to EGFR-TKI. Molecular alterations of EGFR, KRAS, and BRAF genes are more frequent in MP adenocarcinoma than in other pulmonary adenocarcinoma subtypes21. These alterations should be studied in low papillary areas to discern their relationship with MP ACs. Typically, MP cells appear detached and/or connected to alveolar walls lacking a fibrovascular core. Nevertheless, the papillary cells in this study exhibited a clear cellular pattern with the cytoplasm protruding into a glandular cavity, which was the characteristic growth pattern for the MP cells. In light of the similarities between the low papillary and MP patterns in lung adenocarcinomas, can we hypothesize that low papillary areas are early precursors of MP carcinoma and a harbinger for later MP carcinoma development? We compared EGFR statuses and demonstrated that papillary cells with a TKI-resistant mutation feature the same status as adjacent MP cells and even metastasized loci.

Intratumoural EGFR homogeneity in lung cancers has long been assumed. Herein, a patient’s EGFR mutation status was interpreted using a qualitative method, such as sequencing. However, only a fraction of patients harbouring EGFR mutations respond to EGFR-TKIs; thus, additional factors beyond an EGFR-sensitive mutation contribute to a patient’s drug response. In addition to morphological diversity, the potential for remarkable tumour heterogeneity represents a major challenge to personalized medicine and biomarker development24. In the clinical scenario, it could explain the mixed responses to targeted therapies25. Several related biomarkers (e.g., T790M, K-ras, and C-met) have been suspected in EGFR-TKI resistance. Based on recent studies, intratumoural EGFR mutational heterogeneity is a candidate mediator for EGFR-TKI therapy resistance; however, the existence of such heterogeneity remains controversial26,27. The mutations T790M and E20ins are notable resistance mutations and associated with a secondary mutation after EGFR-TKI therapy11. In the current study, sixteen ‘mixed’ ACs harboured sensitive and/or TKI-resistant mutations in addition to 4 histologically pure ACs. Because the primary T790M mutation featured different Ct values than the coexistent sensitive mutation, the LMD and ARMS methods were introduced to analyse the molecular heterogeneity and morphological diversity. The outcomes show that T790M was prevalent in the papillary and MP components, whereas E20ins was more common in the acinar components. However, solid patterns were also observed with acinar patterns in the bulk of the tumour. Cells in the solid area featured an abundant cytoplasm similar to acinar components and harboured the same EGFR status as acinar cells. These outcomes suggest that solid components are paralogous constituents with poor differentiation. In the current study, the EGFR statuses were compared between primary and metastasized foci. Out of the 20 ACs with a TKI-resistant mutation, 13 were metastasized, with at least one component from the primary foci, and featured the same mutation type as the primary tumour. We suspected that these ACs may respond to EGFR-TKI with the same efficacy. However, acinar cells with papillary or MP components exhibited a different EGFR status and a different predominant form. Therefore, the acinar cells were considered a heterogeneous subclone in the tumour cell population. Considering these presentations, we noted that the MP and papillary cells were the most heterogeneous components in lung ACs. Fukutomi et al. reported that MP tumours and low papillary patterns should be differentiated based on morphology to avoid confusing terminology. In brief, a low papillary structure was observed in the lepidic components, whereas a MP pattern was observed in the nonlepidic components. We also observed an extensive lepidic growth pattern in the peripheral area of low papillary cells, especially adjacent to normal lung tissue. EGFR status revealed a congeneric relationship between low papillary and lepidic cells. A low papillary structure is a significant histological feature of the lepidic component and is associated with aggressive cancer behaviour in lung adenocarcinoma28.

Indeed, heterogeneity between primary and metastatic tumours for a limited number of markers (hormonal receptors and HER2 status in breast cancer) has been associated with markedly worse outcomes29,30. Whether these results reflect inappropriate use of targeted therapies or more aggressive tumours with increased genomic instability that produces multiple subclones has not been determined. In our study, a patient at an advanced stage featured a E19del mutation and a minute quantity of T790M without the positive criterion (Ct value ≤28) and received Iressa therapy for 10 months. New progression was observed using computed tomography. Another biopsy was performed, and the EGFR status was determined as an E19del mutation with increasing T790M mutations. The MP pattern persisted with poorer differentiation than before the TKI therapy. This example shows that MP components feature a histological pattern with innate heterogeneity.

Our study suggests that it is critical to determine the heterogeneity of AC components, such as solid, papillary and MP components, by their EGFR status because such components are common in histological subtypes with worse prognoses. Other constituents, such as acinar, may exhibit different molecular features than coexisting papillary or MP cells. Intrinsic heterogeneity is a common biological attribute in MP cells and is an EGFR-TKI resistance mechanism.

Materials and Methods

Excised invasive lung adenocarcinomas were collected at Beijing Chest Hospital from 2013 to 2015. All sample sections were evaluated by two pathologists (YR. Cai and YJ. Dong) to confirm the diagnoses using the 2015 WHO classification criteria and a multi-headed microscope. A mean number of 4.5 slides (range, 1–11 slides) were reviewed, and representative tumour sections were simultaneously determined for further analyses. Histological patterns were calculated though the precise proportions of the components. The clinical stage was defined in accordance with the 7th Edition of the TNM Classification of the Union for International Cancer Control2,31.

DNA extraction, polymerase chain reaction amplification and EGFR mutation assay

Fifty milligrams of tumour tissue from tumour masses was scraped off representative formalin-fixed and paraffin embedded (FFPE) blocks. The EGFR gene status was tested using an amplification refractory mutation system (ARMS) (AmoyDx Inc. Xiamen, China). The genomic DNA extraction and EGFR status assay were performed in accordance with the manufacturer’s protocols (AmoyDx Inc. Xiamen, China).

Diverse phenotypic components of lung adenocarcinoma determined through laser microdissection and EGFR status determined through high-resolution melt curves and ARMS

Typical sections were selected from each specimen both in primary and metastasized loci and were stained with haematoxylin and eosin. Two 6 μm-thick sections were used for laser microdissection (LMD) using a Leica LMD7000 (Leica microsystems, Wetzlar, Germany). Notably, cancer cells with a histological pattern were as pure as possible. If a tumour tissue consisted of cancer cells with different EGFR mutation states, we could determine the relationship between the histological constituents and the genetic attributes. No less than 500 tumour cells from each distinctly histological component were collected, and the DNA was purified using a QIAamp Micro Kit (Cat. No. 56304, Germany) following the manufacturer’s protocol32. Because the genomic DNA quantity was extremely limited in our study, we used high-resolution melt curves (HRMs) to screen the EGFR status, and ARMS was used to determine the mutation type. We used an easy-to-use reaction mix for PCR and a HRM kit (Cat No. 04909631001, Roche, Germany) with a Cobas z 480 PCR amplifier following the manufacturer’s manual with previously described primers33. We compared the HRM curve shapes to screen EGFR status and evaluated the quantity though the cycle threshold value via ARMS.

Ethics approval was obtained from the ethics committee of Beijing Chest Hospital, Capital Medical University, Beijing Tuberculosis and Thoracic Tumour Research Institute and the informed consent was obtained from all subjects. The methods were performed in accordance with the approved procedures from the corresponding manufacturers.

Statistical Analysis

Clinicopathological factors were compared using crosstab χ2 or Fisher’s exact test. We used one-sided and two-sided statistical tests, and the significance level was α = 0.05. All statistical analyses were performed using the JMP system for Windows (version 11, SAS Institute Inc, Cary, NC).

Additional Information

How to cite this article: Cai, Y.-R. et al. Micropapillary: A component more likely to harbour heterogeneous EGFR mutations in lung adenocarcinomas. Sci. Rep. 6, 23755; doi: 10.1038/srep23755 (2016).


  1. 1

    Curado, M. P. E. B., Shin, H. R. et al. Cancer Incidence in Five Continentsed. vol. IX. Lyon: IARC Scientific Publications (2007).

  2. 2

    Travis, W. D. et al. International association for the study of lung cancer/american thoracic society/european respiratory society international multidisciplinary classification of lung adenocarcinoma. J Thorac Oncol 6, 244–285 (2011).

  3. 3

    William, D., Travis, E. B., Allen, P. B., Alexander, Marx, Andrew G. N. (Eds.): WHO Classification of Tumors of the Lung, Pleura, Thymus and Heart (4th edition) Ch.1, 9–152. IARC: Lyon 2015.

  4. 4

    Motoi, N. et al. Lung adenocarcinoma: modification of the 2004 WHO mixed subtype to include the major histologic subtype suggests correlations between papillary and micropapillary adenocarcinoma subtypes, EGFR mutations and gene expression analysis. Am J Surg Pathol 32, 810–827 (2008).

  5. 5

    Sun, Y. et al. Correlation of survival and EGFR mutation with predominant histologic subtype according to the new lung adenocarcinoma classification in stage IB patients. World J Surg Oncol 12, 148 (2014).

  6. 6

    Sica, G. et al. A grading system of lung adenocarcinomas based on histologic pattern is predictive of disease recurrence in stage I tumors. Am J Surg Pathol 34, 1155–1162 (2010).

  7. 7

    Hoshi, R., Tsuzuku, M., Horai, T., Ishikawa, Y. & Satoh, Y. Micropapillary clusters in early-stage lung adenocarcinomas: a distinct cytologic sign of significantly poor prognosis. Cancer 102, 81–86 (2004).

  8. 8

    Watanabe, M. et al. Micropapillary components in a lung adenocarcinoma predict stump recurrence 8 years after resection: a case report. Lung Cancer 80, 230–233 (2013).

  9. 9

    Cha, M. J. et al. Micropapillary and solid subtypes of invasive lung adenocarcinoma: clinical predictors of histopathology and outcome. J Thorac Cardiovasc Surg 147, 921–928 e922 (2014).

  10. 10

    Zhang, Y. et al. A comprehensive investigation of molecular features and prognosis of lung adenocarcinoma with micropapillary component. J Thorac Oncol 9, 1772–1778 (2014).

  11. 11

    Yun, C. H. et al. The T790 M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP. Proc Natl Acad Sci USA 105, 2070–2075 (2008).

  12. 12

    Engelman, J. A. et al. PF00299804, an irreversible pan-ERBB inhibitor, is effective in lung cancer models with EGFR and ERBB2 mutations that are resistant to gefitinib. Cancer Res 67, 11924–11932 (2007).

  13. 13

    Paez, J. G. et al. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 304, 1497–1500 (2004).

  14. 14

    Toyooka, S., Kiura, K. & Mitsudomi, T. EGFR mutation and response of lung cancer to gefitinib. N Engl J Med 352, 2136; author reply 2136 (2005).

  15. 15

    Inukai, M. et al. Presence of epidermal growth factor receptor gene T790 M mutation as a minor clone in non-small cell lung cancer. Cancer Res 66, 7854–7858 (2006).

  16. 16

    Maheswaran, S. et al. Detection of mutations in EGFR in circulating lung-cancer cells. N Engl J Med 359, 366–377 (2008).

  17. 17

    Su, K. Y. et al. Pretreatment epidermal growth factor receptor (EGFR) T790 M mutation predicts shorter EGFR tyrosine kinase inhibitor response duration in patients with non-small-cell lung cancer. J Clin Oncol 30, 433–440 (2012).

  18. 18

    Rosell, R. et al. Pretreatment EGFR T790 M mutation and BRCA1 mRNA expression in erlotinib-treated advanced non-small-cell lung cancer patients with EGFR mutations. Clin Cancer Res 17, 1160–1168 (2011).

  19. 19

    Burgemeister, R. Laser capture microdissection of FFPE tissue sections bridging the gap between microscopy and molecular analysis. Methods Mol Biol 724, 105–115 (2011).

  20. 20

    Warth, A. et al. The novel histologic International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society classification system of lung adenocarcinoma is a stage-independent predictor of survival. J Clin Oncol 30, 1438–1446 (2012).

  21. 21

    De Oliveira Duarte Achcar, R., Nikiforova, M. N. & Yousem, S. A. Micropapillary lung adenocarcinoma: EGFR, K-ras, and BRAF mutational profile. Am J Clin Pathol 131, 694–700 (2009).

  22. 22

    Tsutsumida, H. et al. A micropapillary pattern is predictive of a poor prognosis in lung adenocarcinoma, and reduced surfactant apoprotein A expression in the micropapillary pattern is an excellent indicator of a poor prognosis. Mod Pathol 20, 638–647 (2007).

  23. 23

    Chao, L. et al. Relevance of EGFR mutation with micropapillary pattern according to the novel IASLC/ATS/ERS lung adenocarcinoma classification and correlation with prognosis in Chinese patients. Lung Cancer 86, 164–169 (2014).

  24. 24

    Yap, T. A., Gerlinger, M., Futreal, P. A., Pusztai, L. & Swanton, C. Intratumor heterogeneity: seeing the wood for the trees. Sci Transl Med 4, 127ps110 (2012).

  25. 25

    Turner, N. C. & Reis-Filho, J. S. Genetic heterogeneity and cancer drug resistance. Lancet Oncol 13, e178–185 (2012).

  26. 26

    Gerlinger, M. et al. Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med 366, 883–892 (2012).

  27. 27

    Bai, H. et al. Influence of chemotherapy on EGFR mutation status among patients with non-small-cell lung cancer. J Clin Oncol 30, 3077–3083 (2012).

  28. 28

    Fukutomi, T. et al. Low papillary structures in lepidic lung adenocarcinoma: any relationship with micropapillary lung adenocarcinoma? -reply. Hum Pathol 44, 2867–2868 (2013).

  29. 29

    Liedtke, C. et al. Prognostic impact of discordance between triple-receptor measurements in primary and recurrent breast cancer. Ann Oncol 20, 1953–1958 (2009).

  30. 30

    Niikura, N. et al. Loss of human epidermal growth factor receptor 2 (HER2) expression in metastatic sites of HER2-overexpressing primary breast tumors. J Clin Oncol 30, 593–599 (2012).

  31. 31

    Sobin, L. H. G. M. & Wittekind, C. TNM classification of malignant tumors (UICC International Union Against Cancer). ed. Hoboken, N. J. : Wiley-Blackwell, (2009).

  32. 32

    Burgemeister, R. Nucleic acids extraction from laser microdissected FFPE tissue sections. Methods Mol Biol 724, 117–129 (2011).

  33. 33

    Cai, Y. R. et al. Expression of MET and SOX2 genes in non-small cell lung carcinoma with EGFR mutation. Oncol Rep 26, 877–885 (2011).

Download references


This study was supported by the Beijing Foundation for Distinguished Scientists grant 2009D003013000001 from the Beijing Board of Health.

Author information

Y.C. and Y.D. reviewed the tumour sections and classified the histological types. Y.C. and Z.L. carried out the PCR experiments; L.Z. and D.S. prepared the samples from the formalin-fixed paraffin embedded material and obtained the paraffin sections; X.C., L.Z. and Y.Z. prepared the haematoxylin & eosin stain. Y.C. designed the study and performed the laser microdissection; and Y.C. and Y.D. wrote the paper. H.W. and Y.D. collected clinicopathological data and prepared the figures. All authors discussed the data. All authors reviewed and provided comments to prepare the manuscript.

Correspondence to Yi-Ran Cai.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Cai, Y., Dong, Y., Wu, H. et al. Micropapillary: A component more likely to harbour heterogeneous EGFR mutations in lung adenocarcinomas. Sci Rep 6, 23755 (2016). https://doi.org/10.1038/srep23755

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.